ODCs

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

PROTEIN INTERACTIONS: 1

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

Atypical Mayer-Rokitansky-KÃ¼ster-Hauser syndrome

Macrocephaly-autism syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	WNT4	(0.63)	PTEN

Citations in the biomedical literature:

Atypical Mayer-Rokitansky-KÃ¼ster-Hauser syndrome		Macrocephaly-autism syndrome
	Synonym(s): - Atypical MRKH syndrome - Atypical Rokitansky syndrome - WNT4 deficiency		Synonym(s): (no synonyms)

	Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare endocrine disease - Rare genetic disease - Rare gynecologic or obstetric disease - Rare infertility - Rare renal disease - Rare urogenital disease		Classification (Orphanet): - Rare developmental defect during embryogenesis - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): (no data available)

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

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

No signs/symptoms info available.