Cranial nerves, recurrent paresis of

Preferred Label : Cranial nerves, recurrent paresis of;

Type : Other, mainly phenotypes with suspected mendelian basis;

Inheritance : Autosomal recessive vs. diabetic neuropathy;

Prefixed ID : 218200;

Details

Origin ID

218200;

UMLS CUI

C1857530;

Currated CISMeF NLP mapping
- cranial nerves, recurrent paresis of [MeSH concept]
- cranial nerves, recurrent paresis of [MeSH Supplementary Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Diabetes mellitus [HPO term]
- Facial palsy [HPO term]
- Peripheral neuropathy [HPO term]
- Recurrent external ophthalmoplegia [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- cranial nerves, recurrent paresis of [MeSH Supplementary Concept]
- cranial nerves, recurrent paresis of [MeSH concept]

Keyword's position in hierarchy(ies) :

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