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 |
False |
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 |
Maternally inherited diabetes and deafness (disorder) |
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 |
False |
Genetic disease |
Inferred relationship |
Some |
3 |
Wolfram-like syndrome (disorder) |
Due to |
True |
Genetic disease |
Inferred relationship |
Some |
4 |
Hyperproinsulinaemia |
Associated with |
False |
Genetic disease |
Inferred relationship |
Some |
1 |
Insulin-dependent diabetes mellitus secretory diarrhea syndrome |
Associated with |
False |
Genetic disease |
Inferred relationship |
Some |
1 |
Wolfram syndrome |
Associated with |
False |
Genetic disease |
Inferred relationship |
Some |
3 |
Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome (disorder) |
Due to |
False |
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 |
False |
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 |
False |
Genetic disease |
Inferred relationship |
Some |
|
Prelingual non-syndromic genetic deafness (disorder) |
Is a |
False |
Genetic disease |
Inferred relationship |
Some |
|
Generalised pustular psoriasis |
Is a |
False |
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 |
False |
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 |
False |
Genetic disease |
Inferred relationship |
Some |
|
Primary tethered cord syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Ataxia, photosensitivity, short stature syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Adenocarcinoma of pancreas with neuregulin 1 gene fusion (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Non-small cell lung carcinoma with NRG1 fusion |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Muscular dystrophy |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Malignant tumor of esophagus with NRG1 fusion |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Hadziselimovic syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Female infertility due to genetic disease (disorder) |
Due to |
True |
Genetic disease |
Inferred relationship |
Some |
3 |
Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Cole-Carpenter dysplasia (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Progressive supranuclear palsy |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Chronic diarrhea with villous atrophy syndrome (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Oro-facial digital syndrome type 1 (disorder) |
Is a |
False |
Genetic disease |
Inferred relationship |
Some |
|
Non syndromic camptodactyly of fingers (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Brain malformations, musculoskeletal abnormalities, facial dysmorphism, intellectual disability syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Early-onset progressive encephalopathy, hearing loss, pons hypoplasia, brain atrophy syndrome (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Low density lipoprotein receptor-related protein 5 related primary osteoporosis (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Congenital omphalocele, diaphragmatic hernia, cardiovascular anomalies, radial ray defect syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Camptodactyly syndrome Guadalajara type 3 (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Lethal hydranencephaly, diaphragmatic hernia syndrome (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Maturity-onset diabetes of the young (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Palatal anomalies, widely spaced teeth, facial dysmorphism, developmental delay syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Kosaki overgrowth syndrome (disorder) |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|
Congenital generalized hypercontractile muscle stiffness syndrome |
Is a |
True |
Genetic disease |
Inferred relationship |
Some |
|