LE WE PMID CA
Diabetes mellitus (Hereditary MODY)1821Diabetes mellitus (Hereditaer MODY)

ABCC8 SUR1

Anemia (megaloblastic thiamine responsive)

Bererdinelli Seip congenital lipodystrophy

BSCL1 AGPAT2

BSCL2 Seipin

Diabetes mellitus (Hereditary MODY)

Diabetes mellitus (hereditary)

Diabetes mellitus (neonatal)

Donohue s syndrome Leprechaunism

EIF2AK3 PERK

FRDA1 Frataxin

Friedreich ataxia

Glucokinase

GLUD1

Insulin resistance type a

KCNJ11 Kir6 2

Lipodystrophy

OMIM_601487

OMIM_x600937

Persistent hyperinsulinemic hypoglycemia of infancy

Persistent neonatal hypoglycemia

Rabson Mendenhall s syndrome

Receptor (Insulin)

Receptor (PPAR gamma)

SLC19A2 THTR1

TNDM29locus

Werner s syndrome

Wfs1 Wolframin

Wfs2

Wolcott Rallison syndrome

Wolfram s syndrome DIDMOAD

WRN

2002  
1
Experimental models of transcription factor-associated maturity-onset diabetes of the young.
[12475772] Diabetes 51 Suppl 3(-): S333-42 (2002)
1998  
2
Genetic, metabolic and clinical characteristics of maturity onset diabetes of the young.
[9539292] Eur J Endocrinol 138(3): 233-9 (1998)
2008  
3
Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young.
[18297260] Diabetologia 51(4): 546-53 (2008)
2005  
4
Monogenic syndromes of abnormal glucose homeostasis: clinical review and relevance to the understanding of the pathology of insulin resistance and beta cell failure.
[15772126] J Med Genet 42(12): 893-902 (2005)

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  • Diabetes mellitus (Hereditaer MODY)

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