Disease #01389 (HDR (hypoparathyroidism, sensorineural deafness, and renal dysplasia), OMIM:146255)

Official abbreviation HDR
Name hypoparathyroidism, sensorineural deafness, and renal dysplasia
OMIM ID 146255
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene GATA3
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

2 entries on 1 page. Showing entries 1 - 2.
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00059024 - Karen Avraham laboratory, Tel Aviv university, Israel, unpublished - - no Israel Jewish-Ashkenazi - - - - HDR congenital, moderate-severe hearing loss, kidney disease - GATA3 1 1 Zippi Brownstein
00435323 8300 - - F no Egypt - - - - - HDR hypoparathyroidism sensorineural deafness renal dysplasia GATA3 GATA3 1 1 Manuel Lemos
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