Disease #03303 (DFNB79 (deafness, autosomal recessive, type 79 (DFNB-79)), OMIM:613307)

Official abbreviation DFNB79
Name deafness, autosomal recessive, type 79 (DFNB-79)
OMIM ID 613307
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene TPRN
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00046602 PKDF1129/HLRB6 PubMed: Rehman 2010, Journal: Rehman 2010, PubMed: Naz 2017 5-generation family, 6 affecteds (F, 5M), unaffected heterozygous carriers parents/sibs - yes Pakistan Pakistani - - - - DFNB79 see paper; … TPRN TPRN 1 6 Jacopo Celli
00046603 - PubMed: Khan 2010 7-generation family, 17 affecteds (5F, 12M), unaffected heterozygous carriers parents/sibs - yes Pakistan Pakistani - - - - DFNB79 see paper; … TPRN TPRN 1 17 Jacopo Celli
00046604 - PubMed: Li 2010, Journal: Li 2010 5-generation family, 7 affecteds (6F, M), unaffected heterozygous carriers parents/sibs - yes Morocco Moroccan - - - - DFNB79 see paper; … TPRN TPRN 1 7 Jacopo Celli
00046605 - PubMed: Khan 2010 4-generation family, 4 affecteds (2F, 2M), unaffected heterozygous carriers parents/sibs M yes Pakistan Pakistani - - - - DFNB79 see paper; … TPRN TPRN 1 4 Jacopo Celli
00046606 - PubMed: Khan 2010 5-generation family, 5 affecteds (2F, 3M), unaffected heterozygous carriers parents/sibs - yes Pakistan Pakistani - - - - DFNB79 see paper; … TPRN TPRN 1 5 Jacopo Celli
00046607 - PubMed: Li 2010, Journal: Li 2010 2-generation family, 2 affecteds (F, M), unaffected heterozygous carriers parents - - Netherlands Dutch - - - - DFNB79 see paper; … TPRN TPRN 1 2 Jacopo Celli
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