Cranial nerves, congenital paresis of

Preferred Label : Cranial nerves, congenital paresis of;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal recessive;

Prefixed ID : %218100;

Détails

Origin ID

218100;

UMLS CUI

C1857531;

Currated CISMeF NLP mapping
- cranial nerves, congenital paresis of [MeSH concept]
- cranial nerves, congenital paresis of [MeSH Supplementary Concept]
HPO term(s)
- Abnormality of the pinna [HPO term]
- Autosomal recessive inheritance [HPO term]
- Facial palsy [HPO term]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- cranial nerves, congenital paresis of [MeSH Supplementary Concept]
- cranial nerves, congenital paresis of [MeSH concept]

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