WNT4:Ensemblv115

Wnt family member 4
OMIM: 603490, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Amber WNT4 in Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Amber
Phenotypes
  • Mullerian aplasia and hyperandrogenism (MIM#158330)

Red WNT4 in Osteogenesis Imperfecta and Osteoporosis


Level 2: Skeletal disorders; Endocrine disorders
Version 2.0

1 review Unknown
Sources
  • Expert list
Phenotypes
  • Osteoporosis