NSMF

NMDA receptor synaptonuclear signaling and neuronal migration factor
OMIM: 608137, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red NSMF in Hypogonadotropic hypogonadism

Level 3: Hypothalamic and pituitary disorders
Level 2: Endocrine disorders
Version 1.41

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Radboud University Medical Center, Nijmegen
  • Emory Genetics Laboratory
  • OMIM
Phenotypes
  • Hypogonadotropic hypogonadism 9 with or without anosmia, OMIM:614838
Tags
  • monogenic-polygenic
Red NSMF in Hypogonadotropic hypogonadism (GMS)


Version 3.18
Latest signed off version: v3.0 (22 Mar 2023)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Wessex and West Midlands GLH
  • NHS GMS
  • South West GLH
Phenotypes
  • Hypogonadotropic hypogonadism 9 with or without anosmia, OMIM:614838
Red NSMF in Fetal anomalies


Version 3.157
Latest signed off version: v3.0 (22 Mar 2023)

review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
  • Expert Review Red
  • PAGE Additional Gene List
Phenotypes
  • Hypogonadotropic hypogonadism 9 with or without anosmia, OMIM:614838