PanelApp (test)
  1. Genes and Genomic Entities
  2. WNT7B:Ensemblv115

WNT7B:Ensemblv115

Wnt family member 7B
OMIM: 601967, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green WNT7B in Anophthalmia_Microphthalmia_Coloboma


Level 2: Ophthalmological disorders
Version 2.0

2 reviews BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Green
Phenotypes
  • Pulmonary hypoplasia, Diaphragmatic anomalies, Anophthalmia/microphthalmia and Cardiac defects syndrome
  • Multiple congenital anomalies/dysmorphic features syndrome MONDO:0043005, WNT7B-related

Green WNT7B in Congenital diaphragmatic hernia


Level 2: Dysmorphic and congenital abnormality syndromes
Version 2.0

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Literature
  • Expert Review Green
Phenotypes
  • Pulmonary hypoplasia, Diaphragmatic anomalies, Anophthalmia/microphthalmia and Cardiac defects syndrome
  • Multiple congenital anomalies/dysmorphic features syndrome MONDO:0043005, WNT7B-related