Otosclerosis 7

Preferred Label : Otosclerosis 7;

Symbol : OTSC7;

CISMeF acronym : OTSC7;

Type : Phenotype or locus, molecular basis unknown;

Description : For a phenotypic description and a discussion of genetic heterogeneity of otosclerosis, see OTSC1 (166800).;

Inheritance : Autosomal dominant;

Prefixed ID : %611572;

Details

Origin ID

611572;

UMLS CUI

C1969044;

Currated CISMeF NLP mapping
- otosclerosis 7 [MeSH concept]
- otosclerosis 7 [MeSH Supplementary Concept]
DO Cross reference
- otosclerosis [DO Concept]
HPO term(s)
- Abnormality of the acoustic reflex [HPO term]
- Autosomal dominant inheritance [HPO term]
- Childhood onset sensorineural hearing impairment [HPO term]
- Conductive hearing impairment [HPO term]
- Hearing impairment [HPO term]
- Otosclerosis [HPO term]
- Progressive hearing impairment [HPO term]
ORDO concept(s)
- Familial otosclerosis [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- otosclerosis 7 [MeSH Supplementary Concept]
- otosclerosis 7 [MeSH concept]

Keyword's position in hierarchy(ies) :

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