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Hydranencephaly
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Microtia
2 OMIM references -
1 associated gene
No signs/symptoms info
Hydranencephaly
Microtia

NDE1
(UniProt - OMIM)
 HOXA2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NDE1
(0.63)
HOXA2


Citations in the biomedical literature:


Hydranencephaly
NDE1
Microtia
HOXA2



Hydranencephaly
Microtia

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare otorhinolaryngologic disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
No OMIM references
1 MeSH reference: D006832
External references:
2 OMIM references -
1 MeSH reference: C537772
No signs/symptoms info available.