Facial paresis, hereditary congenital, 2

Preferred Label : Facial paresis, hereditary congenital, 2;

Symbol : HCFP2;

CISMeF acronym : HCFP2; MBS3;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Moebius syndrome 3; MBS3; Mobius syndrome 3;

Description : For a phenotypic description and a discussion of genetic heterogeneity of hereditary congenital facial paresis (HCFP), see 601471.;

Inheritance : Autosomal dominant;

Prefixed ID : %604185;

Details

Origin ID

604185;

UMLS CUI

C1858717;

HPO term(s)
- Autosomal dominant inheritance [HPO term]
- Facial palsy [HPO term]
- Hearing impairment [HPO term]
- Heterogeneous [HPO term]
- Nonprogressive [HPO term]
ORDO concept(s)
- Congenital hereditary facial paralysis-variable hearing loss syndrome [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Facial paresis, hereditary, congenital [MeSH concept]
- facial paresis, hereditary, congenital [MeSH Supplementary Concept]

Keyword's position in hierarchy(ies) :

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