Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Bamforth Lazarus syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Bartsocas Papas syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Congenital cataract with deafness and hypogonadism syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Congenital cataract with hypertrichosis and intellectual disability syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Congenital cataract, nephropathy, encephalopathy syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Catel Manzke syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Congenital hereditary facial paralysis with variable hearing loss syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Congenital intrauterine infection-like syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Congenital lethal erythroderma |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Oculogastrointestinal muscular dystrophy |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hennekam Beemer syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Intellectual disability, hypoplastic corpus callosum, preauricular tag syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Ganglioside GM3 synthase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Ectodermal dysplasia with blindness syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Fuhrmann syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Galloway Mowat syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Orofaciodigital syndrome type 5 |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Osteoporosis and oculocutaneous hypopigmentation syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Pacman dysplasia |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Perlman syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Ackerman syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Agammaglobulinaemia, microcephaly, craniosynostosis, severe dermatitis syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hypoplasia and coloboma of alar cartilage with telecanthus syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Distal limb deficiency with micrognathia syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Duane anomaly, myopathy, scoliosis syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Dystonia 16 |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Ectopia lentis, chorioretinal dystrophy, myopia syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Macular coloboma, cleft palate, hallux valgus syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Toriello Carey syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
LOC syndrome |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Infantile dystonia parkinsonism |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Palmoplantar keratoderma, 46,XX sex reversal, predisposition to squamous cell carcinoma syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Palmoplantar keratoderma Nagashima type |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Glycogen storage disease due to acid maltase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Ethylmalonic encephalopathy |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Endocrine-cerebro-osteodysplasia syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Faciocardiorenal syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Fallot complex with intellectual disability and growth delay syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Familial hypercholanemia |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hypotrichosis with juvenile macular degeneration syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
FADD-related immunodeficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
RIN2 syndrome |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Microbrachycephaly, ptosis, cleft lip syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Microlissencephaly micromelia syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Pili torti onychodysplasia syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Thiamine-responsive encephalopathy |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Tangier disease |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive hyper-IgM syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive retinitis pigmentosa |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Hypotrichosis and intellectual disability syndrome Lopes type |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Microcephalic osteodysplastic dysplasia Saul Wilson type |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Native American myopathy |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Mendelian susceptibility to mycobacterial disease due to complete ISG15 deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Non-eruption of teeth, maxillary hypoplasia, genu valgum syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
PHAVER syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Talo-patello-scaphoid osteolysis syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Spondylocostal dysostosis with anal atresia and genitourinary malformation syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Recessive dystrophic epidermolysis bullosa |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Pierson syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Recessive aplasia cutis congenita of limbs |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Retinal degeneration, nanophthalmos, glaucoma syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Trichothiodystrophy |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Thymic, renal, anal, lung dysplasia syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Steroid dehydrogenase deficiency and dental anomaly syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Split hand, split foot malformation with sensorineural hearing loss syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
SERKAL syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive spastic paraplegia type 44 |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive spastic paraplegia type 46 |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive spastic paraplegia type 53 |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive spastic paraplegia type 54 |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive spastic paraplegia type 57 |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive bestrophinopathy |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive spastic paraplegia type 55 |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Kufor Rakeb syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Seizures and intellectual disability due to hydroxylysinuria syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Schimke immuno-osseous dysplasia |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Richieri Costa Pereira syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Retinohepatoendocrinologic syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Retinal ischaemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Ptosis, upper ocular movement limitation, absence of lacrimal punctum syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Growth delay due to insulin-like growth factor type 1 deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Frontonasal dysplasia with alopecia and genital anomaly syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Familial primary hypomagnesaemia with hypercalciuria and nephrocalcinosis without severe ocular involvement |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
DPM3-CDG - dolichyl-phosphate mannosyltransferase 3 congenital disorder of glycosylation |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Acyl-CoA dehydrogenase 9 deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Autosomal recessive axonal Charcot-Marie-Tooth disease type 2K |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Charcot-Marie-Tooth disease type 2B1 |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Infantile malignant osteopetrosis |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Neuroectodermal melanolysosomal disease |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Nephropathy, deafness, hyperparathyroidism syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Neonatal diabetes, congenital hypothyroidism, congenital glaucoma, hepatic fibrosis, polycystic kidney syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
MPDU1-CDG - mannose-P-dolichol utilisation defect 1 - congenital disorder of glycosylation |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
MOMO syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Mitochondrial myopathy with sideroblastic anaemia syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
Microcephalic primordial dwarfism due to ZNF335 deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|