| 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 | 
| 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 | 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 | 
| 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 | 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 | 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 | 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 |  |