EMB

embigin
OMIM: 615669, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red EMB in Hirschsprung disease


Level 2: Gastroenterological disorders
Version 0.27

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Hirschsprung disease - MONDO:0018309, EMB-related

Red EMB in Mendeliome


Version 1.3795

1 review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Hirschsprung disease - MONDO:0018309, EMB-related