ODCs

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
4 signs/symptoms

Juvenile polyposis of infancy

Persistent MÃ¼llerian duct syndrome

BMPR1A	(UniProt - OMIM)		AMH	(UniProt - OMIM)
PTEN	(UniProt - OMIM)		AMHR2	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PTEN	(0.63)	AMHR2

Citations in the biomedical literature:

Juvenile polyposis of infancy		Persistent MÃ¼llerian duct syndrome
	Synonym(s): - Infantile juvenile polyposis syndrome		Synonym(s): - PMDS - Persistent MÃ¼llerian derivatives

	Classification (Orphanet): - Rare gastroenterologic disease - Rare genetic disease - Rare oncologic disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare infertility - Rare urogenital disease

	Classification (ICD10): - Neoplasms -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: normal Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C536665

Persistent MÃ¼llerian duct syndrome
	Very frequent - Autosomal recessive inheritance - Undescended / ectopic testes / cryptorchidia / unfixed testes Frequent - Inguinal / inguinoscrotal / crural hernia - Male pseudohermaphrodism / lack of virilisation
Juvenile polyposis of infancy
(no data available)