NSMF

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

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green NSMF in Hypogonadotropic hypogonadism

Level 3: Hypothalamic and pituitary disorders
Level 2: Endocrine disorders
Version 1.33

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Radboud University Medical Center, Nijmegen
  • Emory Genetics Laboratory
  • OMIM
Phenotypes
  • Hypogonadotropic hypogonadism 9 with or without anosmia, 614838
  • Endocrine Disorders including conditions such as hypogonadotropic hypogonadism (with or without anosmia): Sequencing Panel (Emory)
Tags
  • monogenic-polygenic

Red NSMF in Hypogonadotropic hypogonadism idiopathic


Version 1.44
Latest signed off version: v1.4 (4 Mar 2020)

review BIALLELIC, autosomal or pseudoautosomal
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 1.698
Latest signed off version: v1.92 (21 Aug 2020)

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