Deafness, autosomal recessive 105

Preferred Label : Deafness, autosomal recessive 105;

Obsolete resource : true;

Moved to : 608653;

Symbol : DFNB105;

CISMeF acronym : DFNB105;

Type : Phenotype, molecular basis known;

Prefixed ID : 616958;

Details

Origin ID

616958;

UMLS CUI

C4310777;

Automatic exact mappings (from CISMeF team)
- autosomal recessive nonsyndromic deafness 32 [DO Concept]
- cell division cycle 14A [HGNC gene]
CISMeF manual mappings
- autosomal recessive nonsyndromic deafness 105 [DO Concept]
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)
- autosomal recessive nonsyndromic deafness 105 [DO Concept]

Keyword's position in hierarchy(ies) :

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