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Stichting WaihonaPedia

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uuid00yngm2

Namestring
Stichting WaihonaPedia
Legal namestring
Stichting WaihonaPedia
Company typeenum
Private
Founded yearint
2016
Descriptiontext

Stichting WaihonaPedia is a Dutch non-profit foundation (stichting) established in 2016 and headquartered at the Jheronimus Academy of Data Science in 's-Hertogenbosch, Netherlands. The foundation develops and operates WaihonaPedia, a wiki-based online platform that supports patient organizations serving people with rare, often care-intensive conditions. The platform combines three integrated functions: a global Community Network connecting affected families, a Knowledge Base that gathers and preserves condition-specific information, and a Peer Connection Hub providing a safe moderated meeting place. According to disclosed scale metrics, the federation comprises 17 patient organizations across 34 countries with 542 active participants, covering 23 rare conditions and connected to 20 expert centres; content is delivered in 9 languages.

The platform is built on XWiki Enterprise open-source wiki software and offers collaborative editing, themed discussion rooms, and an expert Q&A system where questions are anonymized and verified answers are added to the database. The federation model is the core go-to-market: rare-disease patient organizations join the WaihonaPedia Federation, contribute knowledge and funds, and gain access to peer communities, expert networks, and accumulated content. Stichting WaihonaPedia does not sell subscriptions or seats to end users; the platform is provided free of charge to all participants worldwide. Operating revenue consists of contributions from national patient groups and government project grants (including the multi-year STAP-OP research project with Hogeschool Rotterdam, 2024-2027). The organization is led by Managing Director Rob de Back, with Prof. dr. Rob Heethaar as Chairman of the Board and Antoon Kuijpers as Board Member, supported primarily by volunteers including retired academics, parents, and caregivers.

Short descriptiontext

Stichting WaihonaPedia is a Dutch non-profit foundation that operates a free, multilingual, wiki-based online platform connecting 17 rare-disease patient organizations across 34 countries, supporting affected families, expert Q&A, and knowledge preservation.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
Headquarters's-hertogenbosch, Netherlands
HQ citystring
's-hertogenbosch
HQ countrystring
Netherlands
HQ regionstring
Europe
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
rare disease platform, patient community network, collaborative knowledge sharing, nonprofit health foundation, open source wiki software
Industry1 code
1Disability Services & Independent Living Support
CodeBPAGACAGPrimaryYes
NAICS code3 codes
  • Individual and Family Services6241
  • Services for the Elderly and Persons with Disabilities624120
  • Services for the Elderly and Persons with Disabilities62412
SIC code1 code
  • Services-Social Services8300
Product category
Healthcare Community Platform
Social media profiles1 record
GTM motion1 record

Each record includes

Type, Description, Source

Revenue model2 records
1National Patient Group Contributions
TypeSubscription Recurring
Description

The WaihonaPedia Foundation is funded by national groups around disorders who contribute the money needed to keep the platform available. Using this money, the foundation conducts activities to keep the platform working and resolve technical failures.

waihonapedia.org
2Government Project Grants
TypeLicensing Royalties
Description

Revenue is obtained through projects often funded by the government (project grant) and by national groups around the disorders. This supports software development, innovation, and community activities.

waihonapedia.org
Marketing channels6 records

Each record includes

Title, Type, Stage, Description, Source

Distribution channels1 record

Each record includes

Title, Type, Scope, Target buyer, Description, Source

Cost components5 values
Technology or R&D, Operations, Personnel, Infrastructure, Others
Pricing details1 tier
1Free Community Access
ModelFreemiumBilling cadenceMonthly
Notes

Platform available at no cost to families and patient organizations dealing with rare diseases globally.

waihonapedia.org
GTM typeB2B and B2C
B2B and B2C
Offering typeSoftware
Software
Core offering1 text field

WaihonaPedia is a secure, multilingual online platform built on XWiki Enterprise that supports rare disease patient organizations in managing their communities. It provides a free environment for sharing medical and care information, organizing peer support, arranging contact with experts, and documenting accumulated knowledge and experiences across a federation of 17 patient organizations in 34 countries. The underlying software is developed as open source by the foundation and made available free of charge to participants worldwide in 9 languages.

Differentiator
Functional benefit
Problem solved
Quantifiable outcome1 value
  • 17 patient organization communities across 34 countries working together on 23 rare conditions
Product overview1 text field

WaihonaPedia is a single, unified online platform built on XWiki Enterprise that supports patient organizations in managing communities for rare diseases. The platform offers three integrated core features: a global Community Network for connecting individuals affected by rare conditions, a Knowledge Base for gathering and preserving information, and a Peer Connection Hub for safe interaction. The organization operates through the Stichting WaihonaPedia Foundation, a Dutch non-profit entity based at the Jheronimus Academy of Data Science in 's-Hertogenbosch.

Product and service1 record
1WaihonaPedia Platform
CategoryHealthcare Community Platform
Description

The WaihonaPedia Platform is a well-secured online platform built on XWiki Enterprise that supports patient organizations in managing their community for individuals with rare diseases and their families. It provides a safe environment for sharing information, organizing peer support, arranging contact with experts, and documenting accumulated knowledge and experience. The platform offers a global Community Network, a Knowledge Base for gathering and preserving information, and a Peer Connection Hub for safe interaction. It is accessible in 9 languages (English, Danish, German, Spanish, French, Italian, Dutch, Polish, Portuguese).

Scale indicator5 records

Each record includes

Type, Value, Description, Source

Partnership14 partners
Strategic tierCoreTypeStrategic or Co-development Partner
Description

The foundation is based at the Jheronimus Academy of Data Science in 's-Hertogenbosch, Netherlands. This academic partnership supports the organization's data management and research capabilities for rare disease knowledge.

Strategic tierCoreTypeStrategic or Co-development Partner
Description

Collaboration on the STAP-OP research project studying transition care for young people with syndromes or complex conditions from pediatric to adult healthcare, running from 2024-2027.

3European Federation of Williams Syndrome (FEWS)
Strategic tierMajorTypeStrategic or Co-development Partner
Description

FEWS participates in Federatie WaihonaPedia, spreading knowledge and awareness of Williams syndrome through the platform and sharing resources across European member associations.

waihonapedia.org
4expertisecentrum ENCORE TSC (Erasmus MC Rotterdam)
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Expert centre for Tuberous Sclerosis Complex at Erasmus MC providing clinical care, research, and expert consultations for the TSC patient community.

waihonapedia.org
Strategic tierCoreTypeStrategic or Co-development Partner
Description

Expert centre for Tuberous Sclerosis Complex at UMC Utrecht, one of the world's largest TSC outpatient clinics treating 500 adult patients, providing research and clinical expertise.

Strategic tierMajorTypeStrategic or Co-development Partner
Description

US-based patient organization for Marshall Smith Syndrome participating in WaihonaPedia federation for knowledge sharing and community support.

7Vereniging Cornelia de Lange Syndroom
Strategic tierMajorTypeStrategic or Co-development Partner
Description

Dutch association for Cornelia de Lange syndrome participating in WaihonaPedia federation, organizing events and supporting families.

waihonapedia.org
Strategic tierMajorTypeStrategic or Co-development Partner
Description

Dutch foundation for Tuberous Sclerosis Complex participating in WaihonaPedia federation, managing community events and expert networks.

Strategic tierMajorTypeStrategic or Co-development Partner
Description

Dutch foundation for Kabuki syndrome participating in the WaihonaPedia community.

10Nederlandse Vereniging Williams Beuren Syndroom
Strategic tierMajorTypeStrategic or Co-development Partner
Description

Dutch association for Williams Beuren Syndrome participating in WaihonaPedia federation.

waihonapedia.org
11Vereniging Angelman Syndroom Nederland
Strategic tierMajorTypeStrategic or Co-development Partner
Description

Dutch association for Angelman Syndrome participating in WaihonaPedia federation.

waihonapedia.org
12Stichting Rubinstein-Taybi Syndroom
Strategic tierMajorTypeStrategic or Co-development Partner
Description

Dutch foundation for Rubinstein-Taybi Syndrome participating in WaihonaPedia federation.

waihonapedia.org
Strategic tierMinorTypeStrategic or Co-development Partner
Description

Knowledge centre providing expertise on communication for people with combined visual and hearing impairments, contributing to understanding communication challenges in rare conditions.

14Amsterdam Expertise Centrum Ontwikkelingsstoornissen (AECO)
Strategic tierMinorTypeStrategic or Co-development Partner
Description

Amsterdam expertise centre for developmental disorders participating in research projects with WaihonaPedia.

waihonapedia.org
Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Peers10 records
TypeDirect peer
Description

Orphanet is a European reference portal for rare diseases and orphan drugs, offering a comprehensive knowledge base of rare conditions, expert centres, and patient organizations — directly comparable to WaihonaPedia's rare-disease knowledge and community mission.

TypeBroad incumbent
Description

NORD is a large US-based patient-advocacy umbrella for rare diseases providing information, advocacy, and community programs — overlaps with WaihonaPedia's information-sharing and patient-organization support mission at a much larger scale.

TypeBroad incumbent
Description

PatientsLikeMe operates a large online patient community where members track conditions and share experiences; comparable to WaihonaPedia's peer-connection and patient-experience knowledge-sharing functionality, but at much broader scale.

TypeBroad incumbent
Description

HealthUnlocked provides condition-specific online patient communities and information libraries, paralleling WaihonaPedia's federated model of disease-specific communities with peer support and knowledge sharing.

TypeBroad incumbent
Description

EURORDIS is a European federation of rare-disease patient organizations that convenes communities, produces policy work, and runs RareConnect — a broader-incumbent counterpart to WaihonaPedia's Dutch federation model.

TypeBroad incumbent
Description

Inspire runs a large online patient community platform hosting condition-specific support groups including rare-disease communities, comparable in technology and peer-support model to WaihonaPedia.

TypeBroad incumbent
Description

MedlinePlus is the US National Library of Medicine's public health-information portal providing vetted disease and condition content, comparable to WaihonaPedia's curated knowledge-base role for rare-disease families.

TypeEmerging player
Description

GenomeConnect is a patient-empowerment registry for individuals with rare genetic conditions enabling data sharing with researchers, similar in mission to WaihonaPedia's research collaboration with academic partners.

9RareConnect (EURORDIS)
TypeDirect peer
Description

RareConnect is a EURORDIS-hosted moderated online community network connecting rare-disease patients and families across language boundaries, closely paralleling WaihonaPedia's federated community and multilingual peer-support approach.

TypeEmerging player
Description

MyGene2 is a research-focused platform connecting patients with rare genetic conditions to clinicians and other families, overlapping with WaihonaPedia's expert-Q&A and rare-condition knowledge-sharing for care-intensive syndromes.

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses4 records

Each record includes

Headline, Details, Source

Competitive moat4 records

Each record includes

Type, Details

Key risks4 records

Each record includes

Headline, Details, Source

Key highlights6 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

Named customers5 records

Each record includes

Name, Industry, Type, Use case, Source, UUID

Segment3 records

Each record includes

Title, Type, Primary, Description, Pain point addressed, Use case, Source

Ideal customer profile2 records

Each record includes

Profile, Firmographic size, Sales motion, Sales cycle length, Buying structure, Purchase trigger, Buyer persona, Geography, Industry vertical, Primary use case, Description, Pain points, Evidence proof points, Target buyer

Technology focused
Yes
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Feature3 records

Each record includes

Title, Differentiator, Description, Source

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles3 records

Each record includes

Name, Designation, Designation category, Overview, Profile commentary, Source

No data
No data
Funding overview

Funding stage, Last funding date, Total funding USD

Funding rounds

Each record includes

Round, Amount USD, Date, Pre money valuation, Total investors, Investors, News

Investors

Each record includes

Name, Type, Date of entry, Rounds participated, Website

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

M&A

Each record includes

Name, Acquisition type, Announced date, Completed date, Status, Website, News

Investment

Each record includes

Name, Round, Announced date, Lead investor, Website, News

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Stichting WaihonaPedia

Healthcare Community Platformwaihonapedia.org

Stichting WaihonaPedia is a Dutch non-profit foundation that operates a free, multilingual, wiki-based online platform connecting 17 rare-disease patient organizations across 34 countries, supporting affected families, expert Q&A, and knowledge preservation.

What Stichting WaihonaPedia does

Stichting WaihonaPedia is a Dutch non-profit foundation (stichting) established in 2016 and headquartered at the Jheronimus Academy of Data Science in 's-Hertogenbosch, Netherlands. The foundation develops and operates WaihonaPedia, a wiki-based online platform that supports patient organizations serving people with rare, often care-intensive conditions. The platform combines three integrated functions: a global Community Network connecting affected families, a Knowledge Base that gathers and preserves condition-specific information, and a Peer Connection Hub providing a safe moderated meeting place. According to disclosed scale metrics, the federation comprises 17 patient organizations across 34 countries with 542 active participants, covering 23 rare conditions and connected to 20 expert centres; content is delivered in 9 languages.

The platform is built on XWiki Enterprise open-source wiki software and offers collaborative editing, themed discussion rooms, and an expert Q&A system where questions are anonymized and verified answers are added to the database. The federation model is the core go-to-market: rare-disease patient organizations join the WaihonaPedia Federation, contribute knowledge and funds, and gain access to peer communities, expert networks, and accumulated content. Stichting WaihonaPedia does not sell subscriptions or seats to end users; the platform is provided free of charge to all participants worldwide. Operating revenue consists of contributions from national patient groups and government project grants (including the multi-year STAP-OP research project with Hogeschool Rotterdam, 2024-2027). The organization is led by Managing Director Rob de Back, with Prof. dr. Rob Heethaar as Chairman of the Board and Antoon Kuijpers as Board Member, supported primarily by volunteers including retired academics, parents, and caregivers.

Stichting WaihonaPedia firmographics

Firmographics
Name
Stichting WaihonaPedia
Legal name
Stichting WaihonaPedia
Website
https://waihonapedia.org
Company type
Private
Founded year
2016
Operating status
Operating
Headcount range
1–10 employees
Short description
Stichting WaihonaPedia is a Dutch non-profit foundation that operates a free, multilingual, wiki-based online platform connecting 17 rare-disease patient organizations across 34 countries, supporting affected families, expert Q&A, and knowledge preservation.
Ownership category
akta.pro rank

Stichting WaihonaPedia industry classification

Industry
Product category
Healthcare Community Platform
NAICS
Individual and Family Services (6241), Services for the Elderly and Persons with Disabilities (624120), Services for the Elderly and Persons with Disabilities (62412)
SIC
Services-Social Services (8300)
akta.pro primary industry
Disability Services & Independent Living Support (BPAGACAG)

Keywords

  • Rare disease platform
  • Patient community network
  • Collaborative knowledge sharing
  • Nonprofit health foundation
  • Open source wiki software

Where Stichting WaihonaPedia is headquartered

Location

Headquarters

HQ city
's-hertogenbosch
HQ country
Netherlands
HQ region
Europe

Offices1 record

Markets served

Stichting WaihonaPedia business model

Business model
GTM type
B2B and B2C
Offering type
Software
Cost components
Technology or R&D, Operations, Personnel, Infrastructure, Others

Revenue model

  1. National Patient Group Contributions: The WaihonaPedia Foundation is funded by national groups around disorders who contribute the money needed to keep the platform available. Using this money, the foundation conducts activities to keep the platform working and resolve technical failures.
  2. Government Project Grants: Revenue is obtained through projects often funded by the government (project grant) and by national groups around the disorders. This supports software development, innovation, and community activities.

Pricing tiers

ModelBillingPrice
FreemiumMonthlyFree Community Access

Go-to-market motion1 record

Distribution channels1 record

Marketing channels6 records

Stichting WaihonaPedia product offering

Product offering

Core offering

WaihonaPedia is a secure, multilingual online platform built on XWiki Enterprise that supports rare disease patient organizations in managing their communities. It provides a free environment for sharing medical and care information, organizing peer support, arranging contact with experts, and documenting accumulated knowledge and experiences across a federation of 17 patient organizations in 34 countries. The underlying software is developed as open source by the foundation and made available free of charge to participants worldwide in 9 languages.

Product overview

WaihonaPedia is a single, unified online platform built on XWiki Enterprise that supports patient organizations in managing communities for rare diseases. The platform offers three integrated core features: a global Community Network for connecting individuals affected by rare conditions, a Knowledge Base for gathering and preserving information, and a Peer Connection Hub for safe interaction. The organization operates through the Stichting WaihonaPedia Foundation, a Dutch non-profit entity based at the Jheronimus Academy of Data Science in 's-Hertogenbosch.

Differentiator

Problem solved

Functional benefit

Products and services

  • WaihonaPedia Platform The WaihonaPedia Platform is a well-secured online platform built on XWiki Enterprise that supports patient organizations in managing their community for individuals with rare diseases and their families. It provides a safe environment for sharing information, organizing peer support, arranging contact with experts, and documenting accumulated knowledge and experience. The platform offers a global Community Network, a Knowledge Base for gathering and preserving information, and a Peer Connection Hub for safe interaction. It is accessible in 9 languages (English, Danish, German, Spanish, French, Italian, Dutch, Polish, Portuguese).

Quantifiable outcome

  • 17 patient organization communities across 34 countries working together on 23 rare conditions

Companies that use Stichting WaihonaPedia

Customer profile

Named customers5 records

Segments3 records

Ideal customer profiles2 records

Stichting WaihonaPedia technology and API

Technology

Technology focussed Yes

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Feature3 records

Stichting WaihonaPedia partnerships and signals

Strategic signal

Partnerships

14 partnerships are on record, tiered core, major and minor.

  • Jheronimus Academy of Data SciencecoreStrategic or Co-development PartnerThe foundation is based at the Jheronimus Academy of Data Science in 's-Hertogenbosch, Netherlands. This academic partnership supports the organization's data management and research capabilities for rare disease knowledge.
  • Hogeschool Rotterdam (Hogeschool Rotterdam Kenniscentrum Zorginnovatie)coreStrategic or Co-development PartnerCollaboration on the STAP-OP research project studying transition care for young people with syndromes or complex conditions from pediatric to adult healthcare, running from 2024-2027.
  • European Federation of Williams Syndrome (FEWS)majorStrategic or Co-development PartnerFEWS participates in Federatie WaihonaPedia, spreading knowledge and awareness of Williams syndrome through the platform and sharing resources across European member associations.
  • expertisecentrum ENCORE TSC (Erasmus MC Rotterdam)coreStrategic or Co-development PartnerExpert centre for Tuberous Sclerosis Complex at Erasmus MC providing clinical care, research, and expert consultations for the TSC patient community.
  • expertisecentrum TSC UMCU UtrechtcoreStrategic or Co-development PartnerExpert centre for Tuberous Sclerosis Complex at UMC Utrecht, one of the world's largest TSC outpatient clinics treating 500 adult patients, providing research and clinical expertise.
  • Marshall Smith Syndrome Research FoundationmajorStrategic or Co-development PartnerUS-based patient organization for Marshall Smith Syndrome participating in WaihonaPedia federation for knowledge sharing and community support.
  • Vereniging Cornelia de Lange SyndroommajorStrategic or Co-development PartnerDutch association for Cornelia de Lange syndrome participating in WaihonaPedia federation, organizing events and supporting families.
  • Stichting Tubereuze Sclerosis NederlandmajorStrategic or Co-development PartnerDutch foundation for Tuberous Sclerosis Complex participating in WaihonaPedia federation, managing community events and expert networks.
  • Stichting Kabuki SyndroommajorStrategic or Co-development PartnerDutch foundation for Kabuki syndrome participating in the WaihonaPedia community.
  • Nederlandse Vereniging Williams Beuren SyndroommajorStrategic or Co-development PartnerDutch association for Williams Beuren Syndrome participating in WaihonaPedia federation.
  • Vereniging Angelman Syndroom NederlandmajorStrategic or Co-development PartnerDutch association for Angelman Syndrome participating in WaihonaPedia federation.
  • Stichting Rubinstein-Taybi SyndroommajorStrategic or Co-development PartnerDutch foundation for Rubinstein-Taybi Syndrome participating in WaihonaPedia federation.
  • Kentalis Kenniscentrum DoofblindheidminorStrategic or Co-development PartnerKnowledge centre providing expertise on communication for people with combined visual and hearing impairments, contributing to understanding communication challenges in rare conditions.
  • Amsterdam Expertise Centrum Ontwikkelingsstoornissen (AECO)minorStrategic or Co-development PartnerAmsterdam expertise centre for developmental disorders participating in research projects with WaihonaPedia.

Scale indicators5 records

Recent moves6 records

Expansion highlights4 records

Stichting WaihonaPedia competitors and assessment

Company assessment

Direct peers

  • Orphanet: Orphanet is a European reference portal for rare diseases and orphan drugs, offering a comprehensive knowledge base of rare conditions, expert centres, and patient organizations — directly comparable to WaihonaPedia's rare-disease knowledge and community mission.
  • RareConnect (EURORDIS): RareConnect is a EURORDIS-hosted moderated online community network connecting rare-disease patients and families across language boundaries, closely paralleling WaihonaPedia's federated community and multilingual peer-support approach.

Broad incumbents

  • NORD (National Organization for Rare Disorders): NORD is a large US-based patient-advocacy umbrella for rare diseases providing information, advocacy, and community programs — overlaps with WaihonaPedia's information-sharing and patient-organization support mission at a much larger scale.
  • PatientsLikeMe: PatientsLikeMe operates a large online patient community where members track conditions and share experiences; comparable to WaihonaPedia's peer-connection and patient-experience knowledge-sharing functionality, but at much broader scale.
  • HealthUnlocked: HealthUnlocked provides condition-specific online patient communities and information libraries, paralleling WaihonaPedia's federated model of disease-specific communities with peer support and knowledge sharing.
  • EURORDIS – Rare Diseases Europe: EURORDIS is a European federation of rare-disease patient organizations that convenes communities, produces policy work, and runs RareConnect — a broader-incumbent counterpart to WaihonaPedia's Dutch federation model.
  • Inspire: Inspire runs a large online patient community platform hosting condition-specific support groups including rare-disease communities, comparable in technology and peer-support model to WaihonaPedia.
  • MedlinePlus: MedlinePlus is the US National Library of Medicine's public health-information portal providing vetted disease and condition content, comparable to WaihonaPedia's curated knowledge-base role for rare-disease families.

Emerging players

  • GenomeConnect: GenomeConnect is a patient-empowerment registry for individuals with rare genetic conditions enabling data sharing with researchers, similar in mission to WaihonaPedia's research collaboration with academic partners.
  • MyGene2: MyGene2 is a research-focused platform connecting patients with rare genetic conditions to clinicians and other families, overlapping with WaihonaPedia's expert-Q&A and rare-condition knowledge-sharing for care-intensive syndromes.

Market position

Strengths4 records

Weaknesses4 records

Competitive moat4 records

Key risks4 records

Key highlights6 records

Customer concentration

Stichting WaihonaPedia social profiles

Digital presence

Stichting WaihonaPedia financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Stichting WaihonaPedia leadership team

Management profile

Number of profiles

Profiles3 records

Stichting WaihonaPedia funding detail

Funding detail

Funding overview

Funding rounds

Investors

Funding detail is available on the Subscription and Enterprise plan.Contact sales →

Stichting WaihonaPedia M&A and investment

M&A and investment

M&A

Investments

M&A and investment is available on the Subscription and Enterprise plan.Contact sales →

Frequently asked questions about Stichting WaihonaPedia

What does Stichting WaihonaPedia do?

WaihonaPedia is a secure, multilingual online platform built on XWiki Enterprise that supports rare disease patient organizations in managing their communities. It provides a free environment for sharing medical and care information, organizing peer support, arranging contact with experts, and documenting accumulated knowledge and experiences across a federation of 17 patient organizations in 34 countries. The underlying software is developed as open source by the foundation and made available free of charge to participants worldwide in 9 languages.

Is Stichting WaihonaPedia a public or private company?

Stichting WaihonaPedia is a private company. It is classified as nonprofit foundation owned and is currently operating.

When was Stichting WaihonaPedia founded?

Stichting WaihonaPedia was founded in 2016. It employs 1 to 10 people.

Where is Stichting WaihonaPedia based?

Stichting WaihonaPedia is headquartered in 's-hertogenbosch, Netherlands, in the Europe region.

How does Stichting WaihonaPedia make money?

Two revenue lines are on record. National Patient Group Contributions are the primary driver. The others are government Project Grants.

Who are Stichting WaihonaPedia's main competitors?

Direct peers on record are Orphanet and RareConnect (EURORDIS). Broad incumbents are NORD (National Organization for Rare Disorders), PatientsLikeMe, HealthUnlocked, EURORDIS – Rare Diseases Europe, Inspire and MedlinePlus. Emerging players are GenomeConnect and MyGene2.

Does Stichting WaihonaPedia have an API?

No public API is recorded for Stichting WaihonaPedia.

What industry is Stichting WaihonaPedia in?

Stichting WaihonaPedia's product category is Healthcare Community Platform. Its primary akta.pro industry code is BPAGACAG, Disability Services & Independent Living Support. Its NAICS code is 6241 and its SIC code is 8300.

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