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Microlissencephaly
1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
Idiopathic central precocious puberty
1 associated gene
No signs/symptoms info
Microlissencephaly
Idiopathic central precocious puberty

NDE1
(UniProt - OMIM)
 MKRN3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
NDE1
(0.63)
MKRN3


Citations in the biomedical literature:


Microlissencephaly
NDE1
Idiopathic central precocious puberty
MKRN3



Microlissencephaly
Idiopathic central precocious puberty

Classification (Orphanet):
(no data available)
Classification (Orphanet):
- Rare gynecologic or obstetric disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.