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Genetic transient congenital hypothyroidism
1 associated gene
1 connected disease
No signs/symptoms info
Disease Type of connection
Familial thyroid dyshormonogenesis
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare endocrine disease
- Rare genetic disease
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
Gene symbol UniProt reference OMIM reference
DUOX2 Q9NRD8606759
No signs/symptoms info available.