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Familial hypospadias

4 OMIM references -
2 associated genes
1 sign/symptom

PROTEIN INTERACTIONS: 2

Trichothiodystrophy

4 associated genes
No signs/symptoms info

Familial hypospadias

Trichothiodystrophy

AR	(UniProt - OMIM)		ERCC2	(UniProt - OMIM)
MAMLD1	(UniProt - OMIM)		ERCC3	(UniProt - OMIM)
			GTF2H5	(UniProt - OMIM)
			MPLKIP	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	AR AR	(0.75) (0.56)	ERCC3 ERCC2

Citations in the biomedical literature:

Familial hypospadias		Trichothiodystrophy

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the skin and subcutaneous tissue -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 4 OMIM references - No MeSH references		External references: No OMIM references 2 MeSH references: C536559 / D054463

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