ODCs

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4 OMIM references -
2 associated genes
1 sign/symptom

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Familial hypospadias

Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression

AR	(UniProt - OMIM)		TNK2	(UniProt - OMIM)
MAMLD1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	AR	(0.68)	TNK2

Citations in the biomedical literature:

Familial hypospadias		Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare urogenital disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

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

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		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: 4 OMIM references - No MeSH references		External references: No OMIM references No MeSH references

Familial hypospadias
	Very frequent - Hypospadias / epispadias / bent penis
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
(no data available)