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The portal for rare diseases and orphan drugs

There is no disease so rare
that it does not deserve attention

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Caption : Accreditation = ;

- PORTUGAL
- NORTE
- PORTO
- Molecular diagnosis of Multiple epiphyseal dysplasia (COMP and COL2A1 gene: targeted mutation analysis p.Asp473del for COMP gene and sequencing of the entire coding region for COL2A1 gene)
- CGC Genetics / Centro de Genética Clínica
- More information

Orphanet, the mobile portal for rare diseases - MOBILE HEALTH

Orphanet, the mobile portal for rare diseases - MOBILE HEALTH

Languages:

FR
EN
ES
DE
IT
PT
NL

Orphanet version 4.13.0 - Last updated: 2015-01-25

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