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Familial hypospadias

4 OMIM references -
2 associated genes
1 sign/symptom

PROTEIN INTERACTIONS: 1

46,XX testicular disorder of sex development

3 OMIM references -
3 associated genes
5 signs/symptoms

Familial hypospadias

46,XX testicular disorder of sex development

AR	(UniProt - OMIM)		SOX3	(UniProt - OMIM)
MAMLD1	(UniProt - OMIM)		SOX9	(UniProt - OMIM)
			SRY	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	AR	(0.87)	SRY

Citations in the biomedical literature:

Familial hypospadias		46,XX testicular disorder of sex development
	Synonym(s): (no synonyms)		Synonym(s): - 46,XX testicular DSD - De la Chapelle syndrome - XX, male syndrome

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare urogenital disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare infertility - 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: normal Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 4 OMIM references - No MeSH references		External references: 3 OMIM references - 1 MeSH reference: D058531

Familial hypospadias		46,XX testicular disorder of sex development
	Very frequent - Hypospadias / epispadias / bent penis		Very frequent - Abnormal / polycystic ovaries - Ambiguous genitalia - Late puberty / hypogonadism / hypogenitalism - Small / atrophic / hypoplastic testes / monorchism / microorchidism / anorchia - X-linked recessive inheritance