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Microlissencephaly

1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

Familial hypospadias

4 OMIM references -
2 associated genes
1 sign/symptom

Microlissencephaly

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:

Microlissencephaly		Familial hypospadias

	Classification (Orphanet): (no data available)		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: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown 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: 4 OMIM references - No MeSH references

Familial hypospadias
	Very frequent - Hypospadias / epispadias / bent penis
Microlissencephaly
(no data available)