NLGN1

neuroligin 1
OMIM: 600568, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red NLGN1 in Autism


Version 0.36

review Not set
Sources
  • Expert Review Red
  • SFARI
Red NLGN1 in Non-syndromic familial congenital anorectal malformations

Level 3: Gastrointestinal disorders
Level 2: Gastroenterological disorders
Version 1.9

review Not set
Sources
  • Literature
Phenotypes
  • anorectal malformation