Disease #01287 (IDDM2 (diabetes mellitus, insulin-dependent, type 2 (IDDM2)), OMIM:125852)

Official abbreviation IDDM2
Name diabetes mellitus, insulin-dependent, type 2 (IDDM2)
OMIM ID 125852
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 INS
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-02-15 10:39:19 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00024245 - PubMed: Lim 2014, Journal: Lim 2014 - - ? Finland Finnish - - - - IDDM2 Type 2 Diabetis, Obesity, one of the individuals had bilateral hypoacusis or partial hearing loss, a characteristic often associated with BBS. Two of the homozygotes are obese (body mass index [BMI] = 39.2, age = 70; BMI = 37.73, age = 67), and one of them is overweight (BMI = 28.83, age = 69). The lipid levels for one of the individuals (BMI = 37.7) showed that most of her lipid measurements are in the normal range (total cholesterol = 22nd percentile, low-density lipoprotein = 19th percentile, high-density lipoprotein = 14th percentile), but she has elevated levels of triglycerides in the 91st percentile, consistent with the obesity status. None of the three individuals were reported to have cardinal phenotypes associated with BBS such as polydactyly, intellectual disability, cystic kidney disease, or retinal dystrophy. BBS10 BBS10 1 3 Marianne Vos (LOVD-team)
00435322 28771 - - F no ? (unknown) - - - - - IDDM2 Neonatal insulin-dependent diabetes mellitus, Insulin-resistant diabetes mellitus, Small for gestational age, Motor delay, Absent speech, Intellectual disability, Abnormality of movement, Short stature, Increased serum lactate, Elevated circulating creatine kinase concentration, Rhabdomyolysis, Involuntary movements, Dystonia, Hypertonia, Restlessness INS INS 1 1 Andreas Laner
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