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SERKAL syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
COMMON GENES: 1
Atypical Mayer-Rokitansky-Küster-Hauser syndrome
1 OMIM reference -
1 associated gene
No signs/symptoms info
SERKAL syndrome
Atypical Mayer-Rokitansky-Küster-Hauser syndrome

WNT4
(UniProt - OMIM)
 WNT4
(UniProt - OMIM)

COMMON
GENES 		WNT4


Citations in the biomedical literature:


SERKAL syndrome
WNT4
Atypical Mayer-Rokitansky-Küster-Hauser syndrome



SERKAL syndrome
Atypical Mayer-Rokitansky-Küster-Hauser syndrome

Synonym(s):
- Sex reversion - kidneys, adrenal and lung dysgenesis
Synonym(s):
- Atypical MRKH syndrome
- Atypical Rokitansky syndrome
- WNT4 deficiency
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare endocrine disease
- Rare genetic disease
- Rare urogenital disease
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 (ICD10):
(no data available)
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 recessive
Epidemiological data:
Class of prevalence: unknown
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.