SEMA3D

semaphorin 3D
OMIM: 609907, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Red SEMA3D in Mendeliome


Version 2.0

1 review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Hand and foot malformations
  • Hirschsprung disease

Red SEMA3D in Gastrointestinal neuromuscular disease


Level 2: Gastroenterological disorders
Version 2.0

1 review Unknown
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Hirschsprung disease