| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Hereditary gingival fibromatosis |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Autosomal dominant hereditary disorder |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Familial visceral neuropathy |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Adult hypophosphatasia |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Distal arthrogryposis syndrome |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Crigler-Najjar syndrome |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Retinitis pigmentosa |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Childhood hypophosphatasia |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| HNSHA due to hexokinase deficiency |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Erythropoietic protoporphyria |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Infantile hypophosphatasia |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary spherocytosis |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary hollow viscus myopathy |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Robinow syndrome |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Autosomal recessive hereditary disorder |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Congenital dystrophia brevicollis |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Congenital dystrophia brevicollis (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Non dystrophic myotonia (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| 2-hydroxyglutaric aciduria |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary glucocorticoid resistance (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Familial primary hypomagnesemia with normocalciuria (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary isolated hypoparathyroidism due to impaired parathormone secretion (disorder) |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Camptodactyly and tall stature with scoliosis and hearing loss syndrome (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Bone dysplasia Azouz type |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hypomagnesemia co-occurrent with normocalciuria (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Cataract and microcornea syndrome (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Matthew Wood syndrome |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Dystrophic epidermolysis bullosa nails only (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hypotrichosis, lymphedema, telangiectasia, renal defect syndrome (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary hypotrichosis simplex (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Aplasia cutis congenita with epibulbar dermoid syndrome (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Transient bullous dermolysis of newborn (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary hyperekplexia (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Omodysplasia (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Distal muscular dystrophy |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary anetoderma (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Isolated hereditary congenital facial paralysis (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Acral dystrophic epidermolysis bullosa (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Autosomal spastic paraplegia type 30 (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Insulin resistance - type A |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Best vitelliform macular dystrophy (disorder) |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Fundus albipunctatus |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Colobomatous microphthalmia, rhizomelic dysplasia syndrome (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Waardenburg syndrome |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hartsfield syndrome |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Short stature due to growth hormone secretagogue receptor deficiency |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Genetic hyperferritinemia without iron overload |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Female infertility due to zona pellucida defect (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hyperbiliverdinaemia |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Autosomal systemic lupus erythematosus (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Rare isolated myopia |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Corticosteroid-binding globulin deficiency (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Deafness with onychodystrophy syndrome |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Skin fragility, wooly hair, palmoplantar keratoderma syndrome (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Autosomal spastic paraplegia type 72 |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Charcot-Marie-Tooth disease type 2P (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Bleeding diathesis due to collagen receptor defect |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| 46,XY disorder of sex development, adrenal insufficiency due to cytochrome P450 family 11 subfamily A member 1 deficiency (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary isolated aplastic anemia |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hyperandrogenism due to cortisone reductase deficiency |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Malignant migrating partial seizures of infancy (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Familial congenital mirror movements |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Bifid nose (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Fibrochondrogenesis |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Megacystis, microcolon, hypoperistalsis syndrome |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Brachyolmia |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Treacher Collins syndrome |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary clubbing |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary von Willebrand disease type 2 |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Autoimmune lymphoproliferative syndrome |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Familial long QT syndrome |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Arrhythmogenic right ventricular dysplasia (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Adams-Oliver syndrome |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Blount disease |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Osteogenesis imperfecta type 5 (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Erythrokeratodermia variabilis |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Hypodysfibrinogenaemia |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Combined malonic and methylmalonic aciduria |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Progressive cone-rod dystrophy |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Female infertility due to oocyte meiotic arrest |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Global developmental delay, visual anomalies, progressive cerebellar atrophy, truncal hypotonia syndrome (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Trehalase deficiency |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Aicardi Goutieres syndrome type 1 |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Typical nemaline myopathy |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Actin accumulation myopathy (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Intermediate nemaline myopathy |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Autosomal semi-dominant severe lipodystrophic laminopathy (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Central core disease |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Amyotrophic lateral sclerosis type 1 |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Congenital fibre-type disproportion myopathy due to ACTA1 mutation |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Congenital fiber-type disproportion myopathy due to TPM3 mutation |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Familial cerebral saccular aneurysm (disorder) |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Long QT syndrome type 11 (disorder) |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Long QT syndrome type 10 (disorder) |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Long QT syndrome type 3 (disorder) |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Long QT syndrome type 12 (disorder) |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Long QT syndrome type 13 (disorder) |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
| Long QT syndrome type 4 (disorder) |
Is a |
False |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|