Parent Terms |
Term With Siblings |
Child Terms |
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Acanthosis Nigricans Muscle Cramps Acral Enlargement
Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus
Beare-Stevenson cutis gyrata syndrome
Bone Marrow Failure and Diabetes Mellitus Syndrome
Combined Cerebellar and Peripheral Ataxia with Hearing Loss and Diabetes Mellitus
Crouzon syndrome-acanthosis nigricans syndrome
Diabetes Mellitus, Congenital Autoimmune
Diabetes Mellitus, New-Onset after Transplantation
Diabetes, Deafness, Developmental Delay, and Short Stature Syndrome
Experimental Diabetes Mellitus
Familial Acanthosis Nigricans
Feigenbaum Bergeron Richardson Syndrome
Furukawa Takagi Nakao Syndrome
Insulin-Resistant Diabetes Mellitus, with Acanthosis Nigricans
Lipoatrophy with Diabetes, Hepatic Steatosis, Cardiomyopathy, and Leukomelanodermic Papules
Lymphedema-Distichiasis Syndrome with Renal Disease and Diabetes Mellitus
maturity-onset diabetes of the young +
Microcephaly, Epilepsy, and Diabetes Syndrome +
Mitochondrial Myopathy with Diabetes
Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus
Odontochondrodysplasia 2 with Hearing Loss and Diabetes
pancreatic hypoplasia-diabetes-congenital heart disease syndrome
PINEAL HYPERPLASIA, INSULIN-RESISTANT DIABETES MELLITUS, AND SOMATIC ABNORMALITIES
Premature Aging, Okamoto Type
Premature Atherosclerosis with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease
Pseudoacromegaly with Severe Insulin Resistance
thiamine-responsive megaloblastic anemia syndrome
type 1 diabetes mellitus +
type 2 diabetes mellitus +
Wolfram syndrome, mitochondrial form
Woodhouse-Sakati syndrome
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Synonyms |
Exact Synonyms: |
Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans, Type A
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INSULIN RECEPTOR, DEFECT IN, WITH INSULIN-RESISTANT DIABETES MELLITUS AND ACANTHOSIS NIGRICANS
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IRAN, Type A
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Insulin Receptor Defect with Insulin-Resistant Diabetes Mellitus and Acanthosis Nigricans
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Primary IDs: |
MESH:C562710
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Alternate IDs: |
OMIM:610549
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RDO:0012305
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Xrefs: |
EFO:1001503
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