Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Craniofacial ulnar renal syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Craniosynostosis, anal anomaly, porokeratosis syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Craniosynostosis and intracranial calcification syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Cutaneous photosensitivity and lethal colitis syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Cystic leukoencephalopathy without megalencephaly (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Neuronal ceroid lipofuscinosis due to deficiency of cathepsin D (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Chondrodysplasia with disorder of sex development syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Cervical hypertrichosis and peripheral neuropathy syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Ehlers-Danlos syndrome cardiac valvular type (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Ehlers-Danlos syndrome kyphoscoliotic and deafness type (disorder) |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Ehlers-Danlos syndrome musculocontractural type (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Eiken syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Encephalopathy due to prosaposin deficiency (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Asparagine-linked glycosylation 1 congenital disorder of glycosylation (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Filippi syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Deafness with skeletal dysplasia and lip granuloma syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Frank-Ter Haar syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Asparagine-linked glycosylation 3 congenital disorder of glycosylation (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Asparagine-linked glycosylation 8 congenital disorder of glycosylation (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Asparagine-linked glycosylation 9 congenital disorder of glycosylation (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Alopecia, contracture, dwarfism, intellectual disability syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Amaurosis hypertrichosis syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Cloverleaf skull with multiple congenital anomalies syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Cerebro-oculo-dento-auriculo-skeletal syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Ehlers-Danlos syndrome progeroid type (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Fine Lubinsky syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hair defect with photosensitivity and intellectual disability syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hall Riggs syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Heart defect and limb shortening syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Postaxial polydactyly and intellectual disability syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Deaf blind hypopigmentation syndrome Yemenite type (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Deafness, enamel hypoplasia, nail defect syndrome (disorder) |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Diaphanospondylodysostosis (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Diaphragmatic defect, limb deficiency, skull defect syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hydrolethalus syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hyperinsulinism due to short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Short stature due to primary acid labile subunit deficiency (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Siegler Brewer Carey syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Dermatoosteolysis Kirghizian type (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Component of oligomeric golgi complex 7 congenital disorder of glycosylation (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Component of oligomeric golgi complex 8 congenital disorder of glycosylation (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Congenital cataract, hypertrophic cardiomyopathy, mitochondrial myopathy syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Goldberg Shprintzen megacolon syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hereditary sensory and autonomic neuropathy with deafness and global delay (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hereditary sensory and autonomic neuropathy with spastic paraplegia (disorder) |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hydrocephalus, cardiac malformation, dense bone syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Bifid nose, anorectal anomaly, renal anomaly syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Brain dopamine-serotonin vesicular transport disease (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Intellectual disability, epilepsy, bulbous nose syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hidrotic ectodermal dysplasia Halal type (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hypotonia cystinuria syndrome (disorder) |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hirschsprung disease with deafness and polydactyly syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hirschsprung disease with nail hypoplasia and dysmorphism (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Homocystinuria without methylmalonic aciduria (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Familial hypertryptophanemia (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Growth retardation, alopecia, pseudoanodontia, optic atrophy syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hypomandibular faciocranial dysostosis (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder) |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Mendelian susceptibility to mycobacterial disease due to complete interferon gamma receptor 2 deficiency (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Puerto Rican infant hypotonia syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Robinow-like syndrome |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Bilateral microtia with deafness and cleft palate syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Blepharophimosis, ptosis, esotropia, syndactyly, short stature syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hypergonadotropic hypogonadism with cataract syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Lipodystrophy, intellectual disability, deafness syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Lung agenesis with heart defect and thumb anomaly syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Lymphedema, atrial septal defect, facial changes syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Deafness, onychodystrophy, osteodystrophy, intellectual disability syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Deafness and myopia syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Chronic atrial and intestinal dysrhythmia (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Multiple mitochondrial dysfunctions syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hepatic lipase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Adult polyglucosan body disease (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Component of oligomeric golgi complex 5 congenital disorder of glycosylation (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Combined immunodeficiency due to calcium release activated calcium channel dysfunction (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Juvenile primary lateral sclerosis (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hypertelorism with microtia and facial clefting syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Epiphyseal dysplasia, microcephalus, nystagmus syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Intellectual disability with cataract and kyphosis syndrome |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Iron-refractory iron deficiency anemia (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Kapur Toriello syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Kallman syndrome with heart disease (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Obesity due to prohormone convertase I deficiency (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Oculopalatocerebral syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Oculocerebrofacial syndrome Kaufman type (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Oculocutaneous albinism type 5 (disorder) |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Oculocutaneous albinism type 6 (disorder) |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Oculocutaneous albinism type 7 (disorder) |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Oculoosteocutaneous syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Oculotrichodysplasia (disorder) |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Odontoleukodystrophy (disorder) |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Autoimmune lymphoproliferative syndrome with recurrent viral infection (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Bamforth Lazarus syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive popliteal pterygium syndrome (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|