Disease #01285 (MODY1 (diabetes of the young, maturity-onset, type 1 (MODY-1)), OMIM:125850)

Official abbreviation MODY1
Name diabetes of the young, maturity-onset, type 1 (MODY-1)
OMIM ID 125850
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 4
Phenotype entries for this disease 4
Associated with 1 gene HNF4A
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

4 entries on 1 page. Showing entries 1 - 4.
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00208751 Proband 1-Fam PubMed: Fujiwara 2013 proband, variant detected in father, paternal aunt and paternal grandfather. F ? Japan - - - - insulin MODY1 Elevated hemoglobin A1c (HP:0040217), glycosuria (HP:0003076), hyperglycemia (HP:0003074), postprandial hyperglycemia (HP:0011998), decreased apolipoprotein AI level (HP:0031799), abnormal apolipoprotein level (HP:0025201) HNF4A HNF4A 1 4 Jilani Jawaid
00208851 Proband 2-Fam PubMed: Fujiwara 2013 proband, variant detected in mother and maternal grandfather. Affected two maternal great-uncles. F ? Japan - - - - glibenclamide and metformin MODY1 Elevated hemoglobin A1c HP:0040217, glycosuria HP:0003076 HNF4A HNF4A 1 3 Jilani Jawaid
00363865 177890 - - M ? Germany - - - - - MODY1 Known Shwachman-Diamond syndrome, WH deficiency, now pathol. Glucose tolerance, HbA1c 6.1% CEL CEL 1 1 Andreas Laner
00447911 - - - F - Germany - - - - - MODY1 - GCK, HNF1A, HNF4A, KLF11, NEUROD1, PDX1 HNF4A 1 1 Gemeinschaftspraxis für Humangenetik Dresden
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