Disease #01903 (HOMG3 (hypomagnesemia, type 3, renal (HOMG-3)), OMIM:248250)

Official abbreviation HOMG3
Name hypomagnesemia, type 3, renal (HOMG-3)
OMIM ID 248250
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene CLDN16
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

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00080833 - PubMed: Trujillano 2017 no information from parents - - - - - - - - HOMG3 Hypomagnesemia 3, renal type (OMIM:248250) CLDN16 CLDN16 1 1 Daniel Trujillano
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