Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
DNA instability syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Hereditary disease |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Osteogenesis imperfecta |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Microcystic renal disease |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Syndactyly, nystagmus syndrome due to 2q31.1 microduplication |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Mixed sclerosing bone dystrophy with extra-skeletal manifestation (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Syndactyly, polydactyly, ear lobe syndrome (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Dual specificity tyrosine phosphorylation regulated kinase 1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Myopathy and diabetes mellitus (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Familial temporal lobe epilepsy (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Combined immunodeficiency with granulomatosis |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Conductive deafness, malformed external ear syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Hirschsprung disease, ganglioneuroblastoma syndrome (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Heart defect, tongue hamartoma, polysyndactyly syndrome (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Taurodontism |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Lissencephaly with cerebellar hypoplasia type E |
Is a |
False |
Genetic disease |
Inferred relationship |
Some |
|
Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A (disorder) |
Is a |
False |
Genetic disease |
Inferred relationship |
Some |
|
Genetic defect of hair shaft (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Solid neoplasm with neurotrophic receptor tyrosine kinase gene fusion |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Genetic disorder of nail (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
21q22.11q22.12 microdeletion syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Rabson-Mendenhall syndrome |
Associated with |
True |
Genetic disease |
Inferred relationship |
Some |
2 |
Myopathy and diabetes mellitus (disorder) |
Associated with |
True |
Genetic disease |
Inferred relationship |
Some |
3 |
Diabetes-deafness syndrome maternally transmitted |
Associated with |
True |
Genetic disease |
Inferred relationship |
Some |
1 |
Diabetes mellitus associated with genetic syndrome |
Associated with |
True |
Genetic disease |
Inferred relationship |
Some |
1 |
Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome (disorder) |
Due to |
True |
Genetic disease |
Inferred relationship |
Some |
3 |
Wolfram-like syndrome (disorder) |
Due to |
True |
Genetic disease |
Inferred relationship |
Some |
4 |
Hyperproinsulinaemia |
Associated with |
True |
Genetic disease |
Inferred relationship |
Some |
1 |
insulinberoende diabetes mellitus, sekretoriskt diarrésyndrom |
Associated with |
False |
Genetic disease |
Inferred relationship |
Some |
1 |
Diabetes mellitus AND insipidus with optic atrophy AND deafness |
Associated with |
True |
Genetic disease |
Inferred relationship |
Some |
3 |
Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome (disorder) |
Due to |
True |
Genetic disease |
Inferred relationship |
Some |
4 |
Impaired glucose tolerance associated with genetic syndrome |
Associated with |
True |
Genetic disease |
Inferred relationship |
Some |
1 |
Hemolytic uremic syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Boomerang dysplasia |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Osteoglophonic dysplasia |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Winchester syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Congenital wooly hair (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Williams syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Maffucci syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Klippel-Feil sequence |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Angelman syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Prader-Willi syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Hallermann-Streiff syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Focal facial dermal dysplasia (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Trinucleotide repeat disorder (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Woodhouse Sakati syndrome |
Associated with |
True |
Genetic disease |
Inferred relationship |
Some |
4 |
Blau syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Generalized glucocorticoid resistance syndrome (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Male infertility of genetic origin |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Cogan-Reese syndrome (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Genetic lipodystrophy (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Malignant melanoma with B-Raf proto-oncogene, serine/threonine kinase V600E mutation (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Familial hematuria (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Isolated familial renal hypomagnesemia |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness |
Associated with |
True |
Genetic disease |
Inferred relationship |
Some |
7 |
Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction |
Associated with |
True |
Genetic disease |
Inferred relationship |
Some |
7 |
Amyotrophic lateral sclerosis, parkinsonism, dementia complex |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Barber-Say syndrome (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Postlingual non-syndromic genetic deafness |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Prelingual non-syndromic genetic deafness (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Generalised pustular psoriasis |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Cerebro-costo-mandibular syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Familial multiple lipomata (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Short rib dysplasia |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Thin ribs, tubular bones, dysmorphism syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Humeroradioulnar synostosis |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Familial lambdoid synostosis |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Capra DeMarco syndrome (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Radioulnar synostosis with microcephaly and scoliosis syndrome (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Solitary median maxillary central incisor syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Acrocephalosyndactyly |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Cloverleaf skull syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Familial isolated clinodactyly of finger (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Emery-Dreifuss muscular dystrophy |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Primary tethered cord syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|