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 Differences of Sex Development


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.293

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Hypogonadotropic hypogonadism 9 with or without anosmia, MIM# 614838

Red NSMF in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Hypogonadotropic hypogonadism 9 with or without anosmia, MIM# 614838

Red NSMF in Callosome


Level 2: Neurology and neurodevelopmental disorders
Version 0.522

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Hypogonadotropic hypogonadism 9 with or without anosmia, MIM# 614838