Optic atrophy--spastic paraplegia syndrome

Preferred Label : Optic atrophy--spastic paraplegia syndrome;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : X-linked;

Prefixed ID : 311100;

Details

Origin ID

311100;

UMLS CUI

C1839565;

Automatic exact mappings (from CISMeF team)
- optic atrophy spastic paraplegia syndrome [MeSH concept]
- optic atrophy spastic paraplegia syndrome [MeSH Supplementary Concept]
HPO term(s)
- Abnormal oral glucose tolerance [HPO term]
- Optic atrophy [HPO term]
- Spastic paraplegia [HPO term]
- X-linked inheritance [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- optic atrophy spastic paraplegia syndrome [MeSH Supplementary Concept]
- optic atrophy spastic paraplegia syndrome [MeSH concept]

Keyword's position in hierarchy(ies) :

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