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Severe neonatal-onset encephalopathy with microcephaly
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Isolated anophthalmia - microphthalmia
7 OMIM references -
7 associated genes
No signs/symptoms info
Severe neonatal-onset encephalopathy with microcephaly
Isolated anophthalmia - microphthalmia

MECP2
(UniProt - OMIM)
 ALDH1A3
(UniProt - OMIM)
GDF3
(UniProt - OMIM)
OTX2
(UniProt - OMIM)
PRSS56
(UniProt - OMIM)
RAX
(UniProt - OMIM)
SOX2
(UniProt - OMIM)
VSX2
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MECP2
(0.63)
SOX2


Citations in the biomedical literature:


Severe neonatal-onset encephalopathy with microcephaly
MECP2
Isolated anophthalmia - microphthalmia
ALDH1A3 GDF3 OTX2 PRSS56 RAX SOX2
VSX2



Severe neonatal-onset encephalopathy with microcephaly
Isolated anophthalmia - microphthalmia

Synonym(s):
- Severe congenital encephalopathy due to MECP2 mutation
Synonym(s):
- Clinical anophthalmia
- Isolated pure microphthalmia
- Primitive anophthalmia
Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
(no data available)
Classification (ICD10):
(no data available)
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: neonatal/infancy
Average age of death: before age 5
Type of inheritance: x-linked recessive
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: neonatal/infancy
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
External references:
7 OMIM references -
No MeSH references
No signs/symptoms info available.