Cerebral sclerosis, diffuse, scholz type

Preferred Label : Cerebral sclerosis, diffuse, scholz type;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : X-linked;

Prefixed ID : 302700;

Details

Origin ID

302700;

UMLS CUI

C1844884;

Currated CISMeF NLP mapping
- cerebral sclerosis, diffuse, scholz type [MeSH concept]
- cerebral sclerosis, diffuse, scholz type [MeSH Supplementary Concept]
False automatic mappings
- X-linked adrenoleukodystrophy [ORDO Disease]
HPO term(s)
- Blindness [HPO term]
- Deafness [HPO term]
- Dementia [HPO term]
- Hearing impairment [HPO term]
- Juvenile onset [HPO term]
- Lower limb muscle weakness [HPO term]
- Spastic paraplegia [HPO term]
- X-linked inheritance [HPO term]
ORDO concept(s)
- X-linked adrenoleukodystrophy [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- cerebral sclerosis, diffuse, scholz type [MeSH Supplementary Concept]
- cerebral sclerosis, diffuse, scholz type [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients