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1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 OMIM reference -
1 associated gene
No signs/symptoms info
Hydranencephaly
Bilateral microtia - deafness - cleft palate

NDE1 HOXA2


INTERACTOME
ASSOCIATIONS

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



Citations in the biomedical literature:


Hydranencephaly
NDE1
Bilateral microtia - deafness - cleft palate
HOXA2



Hydranencephaly
Bilateral microtia - deafness - cleft palate

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare maxillo-facial surgical disease
- Rare otorhinolaryngologic disease

Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
(no data available)

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 recessive

External references:
No OMIM references
1 MeSH reference: D006832
External references:
1 OMIM reference -
No MeSH references

No signs/symptoms info available.