Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hyperproinsulinaemia |
Is a |
False |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Maternally inherited diabetes and deafness (disorder) |
Is a |
True |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Congenital lipoatrophic diabetes |
Is a |
False |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Maturity onset diabetes mellitus in young |
Is a |
False |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Polyglandular autoimmune syndrome, type 2 |
Is a |
False |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pineal hyperplasia AND diabetes mellitus syndrome (disorder) |
Is a |
True |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Wolfram syndrome (disorder) |
Is a |
False |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Renal cysts and diabetes syndrome |
Is a |
False |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Insulin-dependent diabetes mellitus secretory diarrhea syndrome |
Is a |
False |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare, severe, circulatory system disease characterised by premature, diffuse, severe atherosclerosis (including the aorta and renal, coronary, and cerebral arteries), sensorineural deafness, diabetes mellitus, progressive neurological deterioration with cerebellar symptoms and photomyoclonic seizures, and progressive nephropathy. Partial deficiency of mitochondrial complexes III and IV in the kidney and fibroblasts (but not in muscle) may be associated. There have been no further descriptions in the literature since 1994. |
Is a |
False |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Laminopathy type Decaudain Vigouroux |
Is a |
False |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Wolfram-like syndrome |
Is a |
True |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (disorder) |
Is a |
False |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Myopathy and diabetes mellitus (disorder) |
Is a |
True |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Woodhouse Sakati syndrome |
Is a |
True |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Diabetes mellitus due to cystic fibrosis (disorder) |
Is a |
True |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
diabète sucré concomitant et dû à la mucoviscidose |
Is a |
False |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (disorder) |
Is a |
True |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction |
Is a |
True |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus |
Is a |
True |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Intrauterine growth restriction, short stature, early adult-onset diabetes syndrome |
Is a |
True |
Diabetes mellitus associated with genetic syndrome |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|