Spastic diplegia and impaired intellectual development

Preferred Label : Spastic diplegia and impaired intellectual development;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Spastic diplegia, infantile type; Spastic diplegia and mental retardation;

Inheritance : Autosomal recessive;

Prefixed ID : %270600;

Details

Origin ID

270600;

UMLS CUI

C1849139;

Automatic exact mappings (from CISMeF team)
- cerebral palsy [MeSH Descriptor]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Infantile onset [HPO term]
- Intellectual disability [HPO term]
- Spastic diplegia [HPO term]
ORDO concept(s)
- Spastic diplegia, infantile type [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spastic diplegia infantile type [MeSH concept]
- Spastic diplegia, infantile type [ORDO Disease]
- spastic diplegia infantile type [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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