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

Amyotrophic lateral sclerosis-parkinsonism-dementia complex

AR	(UniProt - OMIM)		PARK7	(UniProt - OMIM)
MAMLD1	(UniProt - OMIM)		TRPM7	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	AR	(0.78)	PARK7

Citations in the biomedical literature:

Familial hypospadias		Amyotrophic lateral sclerosis-parkinsonism-dementia complex
	Synonym(s): (no synonyms)		Synonym(s): - Amyotrophic lateral sclerosis-parkinsonism-dementia of Guam - Guam disease - Lytico-Bodig disease - PDALS - Parkinsonism-dementia-ALS complex

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the nervous system -

	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: 1 OMIM reference - No MeSH references

Familial hypospadias
	Very frequent - Hypospadias / epispadias / bent penis
Amyotrophic lateral sclerosis-parkinsonism-dementia complex
(no data available)