ODCs

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4 OMIM references -
2 associated genes
1 sign/symptom

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Familial hypospadias

Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia

AR	(UniProt - OMIM)		BTK	(UniProt - OMIM)
MAMLD1	(UniProt - OMIM)		ELF4	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	AR	(0.72)	BTK

Citations in the biomedical literature:

Familial hypospadias		Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	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: - Average age onset: neonatal/infancy Average age of death: - Type of inheritance: x-linked recessive

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

Familial hypospadias
	Very frequent - Hypospadias / epispadias / bent penis
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
(no data available)