NSMF

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

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 1.6

1 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 1.2302

1 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 0.540

1 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