spastic paraplegia 11, autosomal recessive

Preferred Label : spastic paraplegia 11, autosomal recessive;

MeSH note : Autosomal recessive hereditary spastic paraplegia, complicated with a thin corpus callosum;

MeSH synonym : spastic paraplegia, autosomal recessive, complicated, with thin corpus callosum; spastic paraplegia, autosomal recessive, with mental impairment and thin corpus callosum; Spg11-Related Hereditary Spastic Paraplegia with Thin Corpus Callosum; Autosomal Recessive Spastic Paraplegia Complicated with Thin Corpus Callosum; Autosomal Recessive Spastic Paraplegia with Mental Impairment and Thin Corpus Callosum; Hsp-Tcc; Spastic Paraplegia Type 11;

Details

Origin ID

C537483;

UMLS CUI

C1858479;

CISMeF manual mappings
- Autosomal recessive spastic paraplegia type 11 [ORDO Disease]
- Autosomal recessive spastic paraplegia type 11 (disorder) [SNOMED CT concept]
Currated CISMeF NLP mapping
- Autosomal recessive spastic paraplegia type 11 [ICD-11 More detail]
- Spastic Paraplegia 11 [NCIt concept]
- Spastic paraplegia 11, autosomal recessive [OMIM Phenotype]
- hereditary spastic paraplegia 11 [DO Concept]
MeSH term(s) associated for indexing
- spastic paraplegia, hereditary [MeSH Descriptor]
ORDO relation(s)
- Autosomal recessive spastic paraplegia type 11 [ORDO Disease]
Record concept(s)
- Spastic paraplegia 11, autosomal recessive [MeSH concept]
See also inter- (CISMeF)
- SPG11 vesicle trafficking associated, spatacsin [ORDO Gene]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spastic Paraplegia 11 [NCIt concept]
- Spastic paraplegia 11, autosomal recessive [OMIM Phenotype]

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