Deafness, X-linked 3

Preferred Label : Deafness, X-linked 3;

Symbol : DFNX3;

CISMeF acronym : DFNX3; DFN4;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Deafness, X-linked 4, congenital sensorineural; DFN4;

Inheritance : X-linked form;

Prefixed ID : %300030;

Details

Origin ID

300030;

UMLS CUI

C3888089;

Automatic exact mappings (from CISMeF team)
- X-linked non-syndromic sensorineural deafness type DFN [ORDO Disease]
Broader ORDO disease(s)
- Non-syndromic genetic deafness [ORDO Disease]
Currated CISMeF NLP mapping
- X-linked deafness 3 [DO Concept]
- deafness, X-Linked 3 [MeSH concept]
- deafness, X-Linked 3 [MeSH Supplementary Concept]
DO Cross reference
- X-linked deafness 3 [DO Concept]
HPO term(s)
- Bilateral sensorineural deafness [HPO term]
- Congenital sensorineural hearing impairment [HPO term]
- Congenital severe sensorineural hearing impairment [HPO term]
- X-linked recessive inheritance [HPO term]
ORDO concept(s)
- X-linked non-syndromic sensorineural deafness type DFN [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- deafness, X-Linked 3 [MeSH Supplementary Concept]
Validated automatic mappings to NTBT
- X-linked nonsyndromic deafness [DO Concept]

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