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Axenfeld anomaly
2 OMIM references -
2 associated genes
No signs/symptoms info
COMMON GENES: 1
PROTEIN INTERACTIONS: 1
Ring dermoid of cornea
1 OMIM reference -
1 associated gene
No signs/symptoms info
Axenfeld anomaly
Ring dermoid of cornea

FOXC1
(UniProt - OMIM)
 PITX2
(UniProt - OMIM)
PITX2
(UniProt - OMIM)

COMMON
GENES 		PITX2
INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
FOXC1
(0.76)
PITX2


Citations in the biomedical literature:


Axenfeld anomaly
FOXC1 PITX2
Ring dermoid of cornea



Axenfeld anomaly
Ring dermoid of cornea

Synonym(s):
(no synonyms)

Synonym(s):
- Ring dermoid syndrome
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
Classification (Orphanet):
- Rare eye disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal dominant
External references:
2 OMIM references -
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: C535684
No signs/symptoms info available.