Spastic paraplegia 25, autosomal recessive

Preferred Label : Spastic paraplegia 25, autosomal recessive;

Symbol : SPG25;

CISMeF acronym : SPG25;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Disc herniation with spastic paraplegia, autosomal recessive;

Description : For a phenotypic description and a discussion of genetic heterogeneity of autosomal recessive spastic paraplegia (SPG), see SPG5A (270800).;

Inheritance : Autosomal recessive;

Prefixed ID : %608220;

Details

Origin ID

608220;

UMLS CUI

C2936860;

Currated CISMeF NLP mapping
- Autosomal recessive spastic paraplegia type 25 [ICD-11 More detail]
- Autosomal recessive spastic paraplegia type 25 [ORDO Disease]
- Autosomal recessive spastic paraplegia type 25 (disorder) [SNOMED CT concept]
- Spastic paraplegia 25, autosomal recessive [MeSH concept]
- hereditary spastic paraplegia 25 [DO Concept]
- spastic paraplegia 25, autosomal recessive [MeSH Supplementary Concept]
DO Cross reference
- hereditary spastic paraplegia 25 [DO Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Back pain [HPO term]
- Neck pain [HPO term]
- Spastic paraplegia [HPO term]
- Spinal cord compression [HPO term]
ORDO concept(s)
- Autosomal recessive spastic paraplegia type 25 [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Autosomal recessive spastic paraplegia type 25 [ORDO Disease]
- Autosomal recessive spastic paraplegia type 25 [ICD-11 More detail]
- Autosomal recessive spastic paraplegia type 25 (disorder) [SNOMED CT concept]
- Spastic paraplegia 25, autosomal recessive [MeSH concept]
- hereditary spastic paraplegia 25 [DO Concept]
- spastic paraplegia 25, autosomal recessive [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients