Disease #01463 (ADTKD1;HNFJ1;MCKD2 (kidney disease, tubulointerstitial, autosomal dominant, type 1), OMIM:162000)

Official abbreviation ADTKD1;HNFJ1;MCKD2
Name kidney disease, tubulointerstitial, autosomal dominant, type 1
OMIM ID 162000
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene UMOD
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2026-04-09 10:43:37 +02:00 (CEST)


Individuals

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00475333 24CA05642 - 3-generation family, 7 affecteds (4F, 3M) F yes China Asia 36y - yes no ADTKD1;HNFJ1;MCKD2 - UMOD UMOD 1 7 Sheng-Guang Li
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