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Senter for sjeldne diagnoser

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uuid005bnd5

Namestring
Senter for sjeldne diagnoser
Legal namestring
Nasjonalt senter for sjeldne diagnoser, enhet Gaustad - Oslo universitetssykehus HF
Company typeenum
Private
Founded yearstring
-
Descriptiontext

Senter for sjeldne diagnoser, now formally known as Nasjonalt senter for sjeldne diagnoser, enhet Gaustad (short form: Sjeldensenteret, enhet Gaustad), is a nationwide, interdisciplinary competence center that collects, builds up, and disseminates knowledge about more than 100 rare diagnoses to healthcare professionals, other service providers, patients, and their relatives in Norway. It operates as a designated unit within Oslo University Hospital HF (Oslo universitetssykehus HF), a public health enterprise owned by Helse Sør-Øst RHF, and collaborates formally with the University of Oslo (UiO).

The center's core product portfolio centers on knowledge dissemination rather than clinical service delivery: a diagnosis information library covering all included conditions, scientific publications and research projects, e-learning courses for healthcare professionals, themed information pages, and a podcast called Sjeldenpodden that shares personal stories and current research. It also operates the Ung Face It platform aimed at young people affected by rare diagnoses, maintains a consent-based patient registry (Pasientregister) that supports research and follow-up, and links patients to relevant user associations (Brukerforeninger). Two named editorial leads (Elizabeth Bjurstrøm and Malena Grant-Falch) oversee website content.

The business model is non-commercial: the center is fully funded through Norway's public healthcare system as part of Oslo University Hospital's national and regional services. There is no pricing for patients, no disclosed revenue, no funding rounds, and no private ownership. Distribution is handled through Oslo University Hospital's existing referral infrastructure and the center's own content channels (website, Facebook, podcast, e-learning), with cross-Nordic knowledge exchange supported through the Nordic Hospital University Alliance (NUHA). Headcount is listed at 6 employees, indicating a lean editorial and coordination team rather than a large operational workforce.

Short descriptiontext

Nasjonalt senter for sjeldne diagnoser, enhet Gaustad is a publicly funded Norwegian national competence center within Oslo University Hospital that collects and disseminates knowledge on more than 100 rare diagnoses to healthcare professionals, patients, and their families.

Operating statusenum
Operating
Ownership categoryenum
Headcount rangeband
1–10
akta.pro rankint
HeadquartersOslo, Norway
HQ citystring
Oslo
HQ countrystring
Norway
HQ regionstring
Europe
Markets served

Serves global market

Offices1 record

Each record includes

City, Country, Type, Description, Source

Keyword5 values
rare disease expertise, medical knowledge dissemination, healthcare professional training, patient support services, rare diagnosis information
Industry2 codes
1Independent Diagnostic Testing Facilities (IDTFs) & Multi-Specialty Diagnostic Centers
CodeHLAFAKANPrimaryYes
2Clinical Research Support (CRC/CTA)
CodeEDAOAJAOPrimaryNo
NAICS code2 codes
  • General Medical and Surgical Hospitals622110
  • Professional, Scientific, and Technical Services54
SIC code2 codes
  • Services-Health Services8000
  • Services-Misc Health & Allied Services, Nec8090
Product category
Rare Disease Healthcare Knowledge Services
Marketing channels4 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
Personnel, Operations, Technology or R&D, Marketing or Sales, Others
GTM typeB2B and B2C
B2B and B2C
Offering typeServices
Services
Core offering1 text field

The center is a nationwide, interdisciplinary competence center that collects, builds, and disseminates knowledge about more than 100 rare diagnoses to healthcare personnel, other service providers, patients, and their relatives. It delivers this expertise through diagnosis information resources, courses and events, e-learning courses for healthcare professionals, the Sjeldenpodden podcast, theme pages, the Ung Face It youth platform, a patient registry, and connections to patient associations.

Differentiator
Functional benefit
Problem solved
Product overview1 text field

Nasjonalt senter for sjeldne diagnoser, enhet Gaustad (Sjeldensenteret) is a nationwide interdisciplinary competence center within Oslo University Hospital that serves as the primary hub for knowledge about rare diagnoses in Norway. The center provides a unified portfolio of services including the Sjeldenpodden podcast, comprehensive diagnosis information, e-learning courses for professionals, thematic pages, and the Ung Face It youth platform. The center also maintains a patient registry and connects patients with relevant user associations. The core offering is expertise dissemination and competence building across more than 100 rare diagnoses for healthcare professionals, service providers, patients, and their families.

Product and service1 record
1Nasjonalt senter for sjeldne diagnoser, enhet Gaustad (National Competence Center)
Scale indicator1 record

Each record includes

Type, Value, Description, Source

Partnership2 partners
1Nordic Hospital University Alliance (NUHA)
Strategic tierModerateTypeStrategic or Co-development Partner
Description

Oslo University Hospital is a member of NUHA, the Nordic Hospital University Alliance, together with Iceland, Finland, Sweden, and Denmark. This alliance facilitates cross-border collaboration and knowledge sharing among Nordic university hospitals.

oslo-universitetssykehus.no
Strategic tierCoreTypeStrategic or Co-development Partner
Description

The center operates in collaboration with the University of Oslo (UiO), as indicated by the UiO logo on their website and the joint branding.

Recent move6 records

Each record includes

Date, Type, Title, Description, Source

Expansion highlight4 records

Each record includes

Type, Description

Market position
Strengths4 records

Each record includes

Headline, Details, Source

Weaknesses3 records

Each record includes

Headline, Details, Source

Competitive moat3 records

Each record includes

Type, Details

Key risks4 records

Each record includes

Headline, Details, Source

Key highlights5 records

Each record includes

Headline, Details, Source

Customer concentration

Classification, Details

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
No
API detail
Has APIbool
No

Docs URL, Description

AI maturity
App detail

Has app

Core technology
Revenue estimate
Valuation estimate
Number of profiles
Profiles2 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 →

Senter for sjeldne diagnoser

Rare Disease Healthcare Knowledge Servicessjeldnediagnoser.no

Nasjonalt senter for sjeldne diagnoser, enhet Gaustad is a publicly funded Norwegian national competence center within Oslo University Hospital that collects and disseminates knowledge on more than 100 rare diagnoses to healthcare professionals, patients, and their families.

What Senter for sjeldne diagnoser does

Senter for sjeldne diagnoser, now formally known as Nasjonalt senter for sjeldne diagnoser, enhet Gaustad (short form: Sjeldensenteret, enhet Gaustad), is a nationwide, interdisciplinary competence center that collects, builds up, and disseminates knowledge about more than 100 rare diagnoses to healthcare professionals, other service providers, patients, and their relatives in Norway. It operates as a designated unit within Oslo University Hospital HF (Oslo universitetssykehus HF), a public health enterprise owned by Helse Sør-Øst RHF, and collaborates formally with the University of Oslo (UiO).

The center's core product portfolio centers on knowledge dissemination rather than clinical service delivery: a diagnosis information library covering all included conditions, scientific publications and research projects, e-learning courses for healthcare professionals, themed information pages, and a podcast called Sjeldenpodden that shares personal stories and current research. It also operates the Ung Face It platform aimed at young people affected by rare diagnoses, maintains a consent-based patient registry (Pasientregister) that supports research and follow-up, and links patients to relevant user associations (Brukerforeninger). Two named editorial leads (Elizabeth Bjurstrøm and Malena Grant-Falch) oversee website content.

The business model is non-commercial: the center is fully funded through Norway's public healthcare system as part of Oslo University Hospital's national and regional services. There is no pricing for patients, no disclosed revenue, no funding rounds, and no private ownership. Distribution is handled through Oslo University Hospital's existing referral infrastructure and the center's own content channels (website, Facebook, podcast, e-learning), with cross-Nordic knowledge exchange supported through the Nordic Hospital University Alliance (NUHA). Headcount is listed at 6 employees, indicating a lean editorial and coordination team rather than a large operational workforce.

Senter for sjeldne diagnoser firmographics

Firmographics
Name
Senter for sjeldne diagnoser
Legal name
Nasjonalt senter for sjeldne diagnoser, enhet Gaustad - Oslo universitetssykehus HF
Website
https://sjeldnediagnoser.no
Company type
Private
Operating status
Operating
Headcount range
1–10 employees
Short description
Nasjonalt senter for sjeldne diagnoser, enhet Gaustad is a publicly funded Norwegian national competence center within Oslo University Hospital that collects and disseminates knowledge on more than 100 rare diagnoses to healthcare professionals, patients, and their families.
Ownership category
akta.pro rank

Senter for sjeldne diagnoser industry classification

Industry
Product category
Rare Disease Healthcare Knowledge Services
NAICS
General Medical and Surgical Hospitals (622110), Professional, Scientific, and Technical Services (54)
SIC
Services-Health Services (8000), Services-Misc Health & Allied Services, Nec (8090)
akta.pro primary industry
Independent Diagnostic Testing Facilities (IDTFs) & Multi-Specialty Diagnostic Centers (HLAFAKAN)
akta.pro secondary industry
Clinical Research Support (CRC/CTA) (EDAOAJAO)

Keywords

  • Rare disease expertise
  • Medical knowledge dissemination
  • Healthcare professional training
  • Patient support services
  • Rare diagnosis information

Where Senter for sjeldne diagnoser is headquartered

Location

Headquarters

HQ city
Oslo
HQ country
Norway
HQ region
Europe

Offices1 record

Markets served

Senter for sjeldne diagnoser business model

Business model
GTM type
B2B and B2C
Offering type
Services
Cost components
Personnel, Operations, Technology or R&D, Marketing or Sales, Others

Distribution channels1 record

Marketing channels4 records

Senter for sjeldne diagnoser product offering

Product offering

Core offering

The center is a nationwide, interdisciplinary competence center that collects, builds, and disseminates knowledge about more than 100 rare diagnoses to healthcare personnel, other service providers, patients, and their relatives. It delivers this expertise through diagnosis information resources, courses and events, e-learning courses for healthcare professionals, the Sjeldenpodden podcast, theme pages, the Ung Face It youth platform, a patient registry, and connections to patient associations.

Product overview

Nasjonalt senter for sjeldne diagnoser, enhet Gaustad (Sjeldensenteret) is a nationwide interdisciplinary competence center within Oslo University Hospital that serves as the primary hub for knowledge about rare diagnoses in Norway. The center provides a unified portfolio of services including the Sjeldenpodden podcast, comprehensive diagnosis information, e-learning courses for professionals, thematic pages, and the Ung Face It youth platform. The center also maintains a patient registry and connects patients with relevant user associations. The core offering is expertise dissemination and competence building across more than 100 rare diagnoses for healthcare professionals, service providers, patients, and their families.

Differentiator

Problem solved

Functional benefit

Products and services

  • Nasjonalt senter for sjeldne diagnoser, enhet Gaustad (National Competence Center)

Companies that use Senter for sjeldne diagnoser

Customer profile

Segments3 records

Ideal customer profiles2 records

Senter for sjeldne diagnoser technology and API

Technology

Technology focussed No

API detail

Has API
No
API docs
API detail

Core technology

AI maturity

App detail

Senter for sjeldne diagnoser partnerships and signals

Strategic signal

Partnerships

Two partnerships are on record, tiered moderate and core.

  • Nordic Hospital University Alliance (NUHA)moderateStrategic or Co-development PartnerOslo University Hospital is a member of NUHA, the Nordic Hospital University Alliance, together with Iceland, Finland, Sweden, and Denmark. This alliance facilitates cross-border collaboration and knowledge sharing among Nordic university hospitals.
  • University of Oslo (UiO)coreStrategic or Co-development PartnerThe center operates in collaboration with the University of Oslo (UiO), as indicated by the UiO logo on their website and the joint branding.

Scale indicators1 record

Recent moves6 records

Expansion highlights4 records

Senter for sjeldne diagnoser competitors and assessment

Company assessment

Market position

Strengths4 records

Weaknesses3 records

Competitive moat3 records

Key risks4 records

Key highlights5 records

Customer concentration

Senter for sjeldne diagnoser social profiles

Digital presence

Senter for sjeldne diagnoser financial estimates

Financial estimate

Revenue estimate

Valuation estimate

Senter for sjeldne diagnoser leadership team

Management profile

Number of profiles

Profiles2 records

Senter for sjeldne diagnoser funding detail

Funding detail

Funding overview

Funding rounds

Investors

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

Senter for sjeldne diagnoser 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 Senter for sjeldne diagnoser

What does Senter for sjeldne diagnoser do?

The center is a nationwide, interdisciplinary competence center that collects, builds, and disseminates knowledge about more than 100 rare diagnoses to healthcare personnel, other service providers, patients, and their relatives. It delivers this expertise through diagnosis information resources, courses and events, e-learning courses for healthcare professionals, the Sjeldenpodden podcast, theme pages, the Ung Face It youth platform, a patient registry, and connections to patient associations.

Is Senter for sjeldne diagnoser a public or private company?

Senter for sjeldne diagnoser is a private company. It is classified as state government owned and is currently operating.

When was Senter for sjeldne diagnoser founded?

Senter for sjeldne diagnoser was founded in -1. It employs 1 to 10 people.

Where is Senter for sjeldne diagnoser based?

Senter for sjeldne diagnoser is headquartered in Oslo, Norway, in the Europe region.

Does Senter for sjeldne diagnoser have an API?

No public API is recorded for Senter for sjeldne diagnoser.

What industry is Senter for sjeldne diagnoser in?

Senter for sjeldne diagnoser's product category is Rare Disease Healthcare Knowledge Services. Its primary akta.pro industry code is HLAFAKAN, Independent Diagnostic Testing Facilities (IDTFs) & Multi-Specialty Diagnostic Centers, with a secondary code of EDAOAJAO, Clinical Research Support (CRC/CTA). Its NAICS code is 622110 and its SIC code is 8000.

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