Spastic paraplegia with precocious puberty

Preferred Label : Spastic paraplegia with precocious puberty;

Type : Other, mainly phenotypes with suspected mendelian basis;

Alternative titles and symbols : Precocious puberty with spastic paraplegia;

Inheritance : Autosomal dominant with variable expression;

Prefixed ID : 182820;

Details

Origin ID

182820;

UMLS CUI

C1866850;

Currated CISMeF NLP mapping
- Spastic paraplegia with precocious puberty [MeSH concept]
- Spastic paraplegia with precocious puberty syndrome (disorder) [SNOMED CT concept]
- Spastic paraplegia-precocious puberty syndrome [ORDO Disease]
- spastic paraplegia with precocious puberty [MeSH Supplementary Concept]
ORDO concept(s)
- Spastic paraplegia-precocious puberty syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spastic paraplegia with precocious puberty [MeSH concept]
- Spastic paraplegia-precocious puberty syndrome [ORDO Disease]
- spastic paraplegia with precocious puberty [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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