Spinocerebellar ataxia type 36 (SCA36) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1) characterized by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasiculations, tongue atrophy and hyperreflexia. [ Orphanet:276198 ]

This is just here as a test because I lose it

Term information

database cross reference
  • OMIM:614153 (Orphanet:276198)
  • DOID:0050983 (MONDO:equivalentTo)
  • Orphanet:276198 (OMIM:614153)
  • UMLS:C3472711 (OMIM:614153)
  • ICD10:G11.8 (Orphanet:276198)
  • NCIT:C148316 (MONDO:equivalentTo)
  • SCTID:711158005 (MONDO:equivalentTo)
  • GARD:0012367 (OMIM-shared)
Subsets

ordo_disease

abbreviation
SCA36 [ Orphanet:276198 MONDO:Lexical https://omim.org/entry/614153 ]

definition

Spinocerebellar ataxia type 36 (SCA36) is a subtype of autosomal dominant cerebellar ataxia type 1 (ADCA type 1) characterized by gait and limb ataxia, lower limb spasticity, dysarthria, muscle fasiculations, tongue atrophy and hyperreflexia.

exactMatch

http://linkedlifedata.com/resource/umls/id/C3472711

http://purl.obolibrary.org/obo/NCIT_C148316

http://identifiers.org/omim/614153

http://identifiers.org/snomedct/711158005

http://purl.obolibrary.org/obo/DOID_0050983

http://www.orpha.net/ORDO/Orphanet_276198

has exact synonym

SCA36

spinocerebellar ataxia type 36

Asidan

has related synonym

spinocerebellar ataxia 36

id

MONDO:0013594