LE WE PMID CA
Anemia (megaloblastic thiamine responsive)13013Anaemie (megaloblastär Thiamin responsiv)

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

2005  
1
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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GG: megaloblastic thiamine responsive anemia
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  • Anaemie (megaloblastär Thiamin responsiv)

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