| Inbound Relationships | Type | Active | Source | Characteristic | Refinability | Group | 
| Oguchi's disease (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Hennekam lymphangiectasia-lymphedema syndrome (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Total intestinal aganglionosis (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Schwartz-Jampel syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Juvenile hyaline fibromatosis | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Odontotrichomelic syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Atelosteogenesis type 2 | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Pseudodiastrophic dysplasia | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Saldino-Mainzer dysplasia | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Desbuquois syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Francois syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Metachromatic leukodystrophy, adult type | Is a | False | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Oligohydramnios sequence | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Gelatinous droplike corneal dystrophy (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Brachyolmia - Maroteaux type (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Blomstrand dysplasia (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Raine dysplasia (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Autosomal recessive familial woolly hair | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Autosomal recessive pseudoxanthoma elasticum (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome, recessive type 4 | Is a | False | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Jarcho-Levin syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Achromatopsia | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Seckel syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Diastrophic dysplasia | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Werner syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Diaphragmatic hernia, abnormal face and distal limb anomalies (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Grebe syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Short rib-polydactyly syndrome, Majewski type | Is a | False | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Metaphyseal chondrodysplasia, McKusick type | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Acrofrontofacionasal dysostosis type 2 | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Ehlers-Danlos syndrome, dominant type 4 | Is a | False | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Marinesco-Sjögren syndrome (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Dyggve-Melchior-Clausen syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Alopecia, epilepsy, intellectual disability syndrome Moynahan type | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Focal facial dermal dysplasia type IV (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| SPOAN and SPOAN-related disorder | Is a | False | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Woodhouse Sakati syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| GM1 gangliosidosis | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Amelogenesis imperfecta, pigmented hypomaturation type | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Autosomal recessive hypohidrotic ectodermal dysplasia syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Autosomal recessive progressive external ophthalmoplegia | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Deafness and oligodontia syndrome (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Diffuse mesangial sclerosis with ocular abnormalities | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Enamel-renal syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Renal dysplasia and retinal aplasia | Is a | False | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Renal tubular acidosis with progressive nerve deafness | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Immotile cilia syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Cystic fibrosis | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Cholestasis-edema syndrome, Norwegian type | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Selective malabsorption of cyanocobalamin | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Diabetes mellitus AND insipidus with optic atrophy AND deafness | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Hereditary xanthinuria type 1 | Is a | False | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Hereditary von Willebrand disease type 3 | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Hereditary von Willebrand disease type 2N (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Autosomal recessive optic atrophy type 6 | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Benign intrahepatic cholestasis type 1 | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Severe childhood autosomal recessive muscular dystrophy | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Bartter syndrome (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Hereditary sensory autonomic neuropathy type IIA | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Hereditary sensory autonomic neuropathy type IIB (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Hyperphosphataemic familial tumoural calcinosis | Is a | False | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Syndrome of apparent mineralocorticoid excess | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Perinatal lethal Gaucher disease (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Roberts-SC phocomelia syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Familial pulmonary capillary haemangiomatosis | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Familial hemophagocytic lymphohistiocytosis (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Papuloverrucous palmoplantar keratoderma of Jakac-Wolf | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Alpha-N-acetylgalactosaminidase deficiency type 1 | Is a | False | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Short rib polydactyly syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Alpha-N-acetylgalactosaminidase deficiency type 2 | Is a | False | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Alpha-N-acetylgalactosaminidase deficiency type 3 (disorder) | Is a | False | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Lethal Kniest-like syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Otospondylomegaepiphyseal dysplasia | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Acroerythrokeratoderma | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Rolland-Debuqois syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Acrocardiofacial syndrome (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Pachydermoperiostosis syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Autosomal recessive Robinow syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Bilateral frontoparietal polymicrogyria (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Congenital muscular dystrophy type 1C due to fukutin related protein gene mutation (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Congenital muscular dystrophy type 1D large gene mutation (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Congenital disorder of glycosylation type 1i | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Type 3 lissencephaly | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Phenylketonuria due to tetrahydrobiopterin deficiency | Is a | False | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Rothmund Thomson syndrome type 1 (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Rothmund Thomson syndrome type 2 | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Stickler syndrome type 4 (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Wrinkly skin syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Infantile systemic hyalinosis | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Polyglandular autoimmune syndrome, type 1 | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Acute neuronopathic Gaucher's disease | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Congenital secretory diarrhea, chloride type | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Vanishing white matter disease (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Hemoglobin C beta thalassemia (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Citrullinemia type I (disorder) | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Curry-Hall syndrome | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Progressive cerebellar ataxia with hypogonadism | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  | 
| Hereditary dysautonomia with motor neuropathy | Is a | True | Autosomal recessive hereditary disorder | Inferred relationship | Some |  |