Deafness, autosomal recessive 13

Preferred Label : Deafness, autosomal recessive 13;

Symbol : DFNB13;

CISMeF acronym : DFNB13;

Type : Phenotype or locus, molecular basis unknown;

Inheritance : Autosomal recessive;

Prefixed ID : %603098;

Details

Origin ID

603098;

UMLS CUI

C1864199;

Automatic exact mappings (from CISMeF team)
- Autosomal recessive non-syndromic sensorineural deafness type DFNB [ORDO Disease]
Currated CISMeF NLP mapping
- autosomal recessive nonsyndromic deafness 13 [DO Concept]
- deafness, autosomal recessive 13 [MeSH concept]
- deafness, autosomal recessive 13 [MeSH Supplementary Concept]
DO Cross reference
- autosomal recessive nonsyndromic deafness 13 [DO Concept]
HPO term(s)
- Autosomal recessive inheritance [HPO term]
- Hearing impairment [HPO term]
- Sensorineural hearing impairment [HPO term]
ORDO concept(s)
- Autosomal recessive non-syndromic sensorineural deafness type DFNB [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- deafness, autosomal recessive 13 [MeSH Supplementary Concept]
- deafness, autosomal recessive 13 [MeSH concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients