ODCs

Click node...

4 OMIM references -
2 associated genes
1 sign/symptom

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
No signs/symptoms info

Familial hypospadias

Familial platelet syndrome with predisposition to acute myelogenous leukemia

AR	(UniProt - OMIM)		RUNX1	(UniProt - OMIM)
MAMLD1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	AR	(0.52)	RUNX1

Citations in the biomedical literature:

Familial hypospadias		Familial platelet syndrome with predisposition to acute myelogenous leukemia
	Synonym(s): (no synonyms)		Synonym(s): - FPD/AML syndrome - FPS/AML syndrome - Familial platelet disorder with associated myeloid malignancy - Familial platelet syndrome

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare urogenital disease		Classification (Orphanet): - Rare genetic disease - Rare hematologic disease - Rare oncologic 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: <1 / 1 000 000 Average age onset: no data available Average age of death: no data available Type of inheritance: autosomal dominant

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

Familial hypospadias
	Very frequent - Hypospadias / epispadias / bent penis
Familial platelet syndrome with predisposition to acute myelogenous leukemia
(no data available)