Supranuclear palsy, progressive, 3

Preferred Label : Supranuclear palsy, progressive, 3;

Symbol : PSNP3;

CISMeF acronym : PSNP3;

Type : Phenotype or locus, molecular basis unknown;

Description : For a phenotypic description and a discussion of genetic heterogeneity of progressive supranuclear palsy (PSP), see PSNP1 (601104).;

Prefixed ID : %610898;

Details

Origin ID

610898;

UMLS CUI

C1970476;

Broader ORDO disease(s)
- Progressive supranuclear palsy [ORDO Disease]
Currated CISMeF NLP mapping
- supranuclear palsy, progressive, 3 [MeSH concept]
- supranuclear palsy, progressive, 3 [MeSH Supplementary Concept]
DO Cross reference
- progressive supranuclear palsy [DO Concept]
ORDO concept(s)
- Classic progressive supranuclear palsy syndrome [ORDO Disease]
- Progressive supranuclear palsy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- supranuclear palsy, progressive, 3 [MeSH Supplementary Concept]
- supranuclear palsy, progressive, 3 [MeSH concept]

Keyword's position in hierarchy(ies) :

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