Insulin resistance

syndrome OMIM 615381

Andibular Hypoplasia, Deafness, Progeroid Features, And Lipodystrophy Syndrome

freq: 4/4 ev: PCS

syndrome OMIM 209900

Bardet-Biedl Syndrome 1 (Disorder)

freq: 1/1 ev: PCS

phenotype OMIM 617885

Body Mass Index Quantitative Trait Locus 19

freq: 1/4 ev: PCS

disease OMIM 214150

Cerebrooculofacioskeletal Syndrome 1

freq: 1/3 ev: PCS

syndrome OMIM 614662

Cortisone Reductase Deficiency 2

freq: 1/2 ev: PCS

syndrome OMIM 610549

Diabetes Mellitus, Insulin-Resistant, With Acanthosis Nigricans

freq: 1/1 ev: PCS

syndrome OMIM 612227

Diabetes Mellitus, Ketosis-Prone

ev: TAS

syndrome OMIM 125853

Diabetes Mellitus, Non-Insulin-Dependent

ev: TAS

syndrome OMIM 151660

Familial Partial Lipodystrophy, Type 2

freq: 6/6 ev: PCS

syndrome OMIM 604367

Familial Partial Lipodystrophy, Type 3

freq: 3/3 ev: PCS

disease OMIM 125853

Insulin Resistance, Susceptibility To

ev: TAS

syndrome OMIM 612526

Lipodystrophy, Congenital Generalized, Type 3

ev: PCS

syndrome OMIM 613327

Lipodystrophy, Congenital Generalized, Type 4

ev: IEA

syndrome OMIM 613877

Lipodystrophy, Familial Partial, Type 4

freq: 3/3 ev: PCS

syndrome OMIM 615980

Lipodystrophy, Familial Partial, Type 6

ev: TAS

syndrome OMIM 615703

Morbid Obesity And Spermatogenic Failure

ev: TAS

syndrome OMIM 606721

Partial Lipodystrophy, Congenital Cataracts, And Neurodegeneration Syndrome

freq: 1/3 ev: PCS

syndrome OMIM 617253

Seckel Syndrome 10

freq: 2/2 ev: PCS

syndrome OMIM 616541

Short Stature, Microcephaly, And Endocrine Dysfunction

ev: TAS

syndrome OMIM 269880

Short Syndrome

freq: 7/7 ev: PCS