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autosomal recessive nonsyndromic hearing loss 63

Go to external page http://purl.obolibrary.org/obo/MONDO_0012670

Any autosomal recessive nonsyndromic deafness in which the cause of the disease is a mutation in the LRTOMT gene. [ MONDO:patterns/disease_series_by_gene ]

Synonyms: autosomal recessive nonsyndromic hearing loss 63

This is just here as a test because I lose it

Term information

database cross reference
Subsets

gard_rare, rare, nord_rare, clingen

IAO 0000233

https://github.com/monarch-initiative/mondo/issues/551

https://github.com/monarch-initiative/mondo/issues/4521

exactMatch

https://omim.org/entry/611451

http://purl.obolibrary.org/obo/DOID_0110515

http://linkedlifedata.com/resource/umls/id/C1969621

http://identifiers.org/mesh/C566951

has narrow synonym

autosomal recessive nonsyndromic deafness 63

autosomal recessive nonsyndromic deafness caused by mutation in LRTOMT

deafness, autosomal recessive 63

LRTOMT autosomal recessive nonsyndromic deafness

deafness, autosomal recessive type 63

autosomal recessive deafness 63

DFNB63

autosomal recessive nonsyndromic deafness type 63

id

MONDO:0012670

seeAlso

https://search.clinicalgenome.org/kb/conditions/MONDO:0012670

Term relations