Disease #00394 (HOMG1 (hypomagnesemia 1, intestinal), OMIM:602014)

Official abbreviation HOMG1
Name hypomagnesemia 1, intestinal
OMIM ID 602014
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 8
Phenotype entries for this disease 8
Associated with 1 gene TRPM6
Associated tissues -
Disease features -
Remarks -
Date created 2014-05-30 14:05:18 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

8 entries on 1 page. Showing entries 1 - 8.
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00016698 - PubMed: Schlingmann 2002 5-generation family, 2 affecteds (F1.1, F1.2), unaffected carriers F yes Turkey white - - - - HOMG1 initial Mg2+ 0.21 mM, FE Mg2+ 4.8%; age onset 9w TRPM6 TRPM6 1 1 Karl Schlingmann
00016701 - PubMed: Schlingmann 2002 4-generation family, 1 affected, unaffected carrier parents M yes Turkey white - - - - HOMG1 initial Mg2+ 0.08 mM, FE Mg2+ 2.8%; age onset 3w TRPM6 TRPM6 1 1 Karl Schlingmann
00016705 - PubMed: Schlingmann 2002 - F - Sweden white - - - - HOMG1 initial Mg2+ 0.10 mM, FE Mg2+ 4.0% TRPM6 TRPM6 2 1 Karl Schlingmann
00016707 - PubMed: Schlingmann 2002 - ? no Israel Jewish - - - - HOMG1 initial Mg2+ 0.41 mM, FE Mg2+high; age onset 4w TRPM6 TRPM6 2 1 Karl Schlingmann
00016708 - PubMed: Schlingmann 2002 4-generation family, 2 affected sisters (F5.1/F5.2), unaffected carrier parents F yes Albania white - - - - HOMG1 initial Mg2+ 0.17 mM, FE Mg2+ 4.5%; age onset 5w TRPM6 TRPM6 1 1 Karl Schlingmann
00016843 - PubMed: Schlingmann 2002 4-generation family, 2 affected sisters (F5.1/F5.2), unaffected carrier parents F yes Albania - - - - - HOMG1 initial Mg2+ 0.22 mM, FE Mg2+ 2.6%; age onset 5w TRPM6 TRPM6 1 1 Karl Schlingmann
00231400 John Sayer - - F yes Oman - 05y - - - HOMG1 hypomagnesemia (HP:0002917), hypocalcaemia (HP:0002901) TRPM6 TRPM6 1 3 John Sayer
00414236 201120 - - F likely Germany - - - - - HOMG1 Hypomagnesemia, Seizure TRPM6 TRPM6 1 1 Andreas Laner
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