Terminology Service for NFDI4Health

Infantile Neuroaxonal Dystrophy

Go to external page http://purl.obolibrary.org/obo/NCIT_C84927


A rare autosomal recessive neurodegenerative disorder caused by mutations in the PLA2G6 gene. It is characterized by the development of swellings called spehroids along the axons of the central nervous system. Signs and symptoms appear early in life and include movement difficulties, muscle hypotonia and spasticity, and dementia. [ ]

Term info

Label

Infantile Neuroaxonal Dystrophy

Synonyms
  • Infantile Neuroaxonal Dystrophy
Preferred Name

Infantile Neuroaxonal Dystrophy

Semantic Type

Disease or Syndrome

UMLS CUI

C0270724

code

C84927