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Hydranencephaly
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Familial hypospadias
4 OMIM references -
2 associated genes
1 sign/symptom
Hydranencephaly
Familial hypospadias

NDE1
(UniProt - OMIM)
 AR
(UniProt - OMIM)
MAMLD1
(UniProt - OMIM)

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


Citations in the biomedical literature:


Hydranencephaly
NDE1
Familial hypospadias
AR MAMLD1



Hydranencephaly
Familial hypospadias

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare urogenital 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: unknown
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:
4 OMIM references -
No MeSH references
Familial hypospadias

Very frequent
- Hypospadias / epispadias / bent penis



Hydranencephaly

(no data available)