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 |
True |
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 |
|
skelettdysplasi, typ Azouz |
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's syndrome |
Is a |
True |
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 |
|
von Willebrand disease type 2 |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
Autoimmune lymphoproliferative syndrome |
Is a |
True |
Autosomal hereditary disorder |
Inferred relationship |
Some |
|
Congenital long QT syndrome (disorder) |
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 |
|