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Canavan disease

Disease Summary
Associated Targets (2)
Tbio

2


GARD Rare
Mondo Description Canavan disease (CD) is a neurodegenerative disorder; its spectrum varies between severe forms with leukodystrophy, macrocephaly and severe developmental delay, and a very rare mild/juvenile form characterized by mild developmental delay.
Uniprot Description A rare neurodegenerative condition of infancy or childhood characterized by white matter vacuolization and demyelination that gives rise to a spongy appearance. The clinical features are onset in early infancy, atonia of neck muscles, hypotonia, hyperextension of legs and flexion of arms, blindness, severe mental defect, megalocephaly, and death by 18 months on the average.
Mondo Term and Equivalent IDs
MONDO:0010079:  Canavan disease
GARD:0005984: 
MESH:D017825: 
NCIT:C84611: 
Orphanet:141: 
SCTID:80544005: 
UMLS:C0206307: