| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Resistance to thyroid hormone due to mutation in thyroid hormone receptor beta |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Polyendocrine polyneuropathy syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Infantile multisystem neurologic, endocrine, pancreatic disease |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary methaemoglobinaemia, enzymatic type |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Deficiency of AMP pyrophorylase |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Familial erythrocytosis due to diphosphoglycerate mutase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Medium-chain acyl-coenzyme A dehydrogenase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Cystinosis |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Autosomal recessive severe combined immunodeficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Pseudocholinesterase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Autosomal recessive hypophosphataemic bone disease |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Transcobalamin II deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Familial chronic mucocutaneous candidiasis - recessive type |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Methylcrotonyl-CoA carboxylase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Geroderma osteodysplastica |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Propionyl-CoA carboxylase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Childhood hypophosphatasia |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Alpha-1 antitrypsin deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Essential benign fructosuria |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Glucocorticoid deficiency with achalasia |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Infantile hypophosphatasia |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Alkaptonuria |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Adenylosuccinate lyase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Biotin-(propionyl-CoA-carboxylase) ligase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Mule foot deformity |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Jervell and Lange-Nielsen syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Severe steroid 21-hydroxylase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Autosomal recessive asexual dwarfism |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Iodotyrosine deiodination defect |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Primary hyperoxaluria |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary fructose intolerance |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Beta-aminoisobutyric aciduria |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Arginase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Cystathionine beta-synthase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Galactosylceramide lipidosis |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| 5-Oxoprolinase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Chorea acanthocytosis syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Westphal-Strumpell syndrome |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Maple syrup urine disease |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Pyle metaphyseal dysplasia |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Methylene THF reductase deficiency AND homocystinuria |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Fructose-1,6-bisphosphatase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Methylmalonyl-CoA mutase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Wilson's disease * |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Glycogen storage disease |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Acetyl-CoA: acyltransferase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Spondyloenchondromatosis |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Giacci familial neurogenic acroosteolysis |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Testicular tumour of adrenogenital syndrome |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Jervell and Lange-Nielson syndrome |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| HNSHA due to pyrimidine-5'-nucleotidase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Glutamate-cysteine ligase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary factor X deficiency disease |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary acrodermatitis enteropathica |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Morquio syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Lipid proteinosis |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Sialidosis |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Propionyl-CoA carboxylase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Glutathione synthase deficiency with 5-oxoprolinuria |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Familial C3B inhibitor deficiency syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Papillon-Lefèvre syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Sulfite oxidase deficiency syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Argininosuccinate lyase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| 5,10-Methylenetetrahydrofolate reductase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary factor XII deficiency disease |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Mucopolysaccharidosis, MPS-VII |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Cholesterol monooxygenase (side-chain cleaving) deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Dubin-Johnson syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Xeroderma pigmentosum |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Adenosine deaminase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Propionic acidaemia |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Acetyl-CoA: acyltransferase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Orotic aciduria |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Hypervalinaemia |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Corticosterone 18-monooxygenase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Hypertyrosinaemia, Richner-Hanhart type |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Phosphatidylcholine-sterol acyltransferase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Succinate-semialdehyde dehydrogenase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary factor XI deficiency disease |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Testosterone 17-beta-dehydrogenase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| HNSHA due to glutathione reductase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| HNSHA due to glucose phosphate isomerase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Steroid 21-monooxygenase deficiency, simple virilising type |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Congenital lactase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| 3 beta-Hydroxysteroid dehydrogenase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Multiple sulfatase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Aspartylglucosaminuria |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Craniodiaphyseal dysplasia |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Ehlers-Danlos syndrome, procollagen proteinase deficient |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Essential benign pentosuria |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Bardet-Biedl syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Cohen syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Intestinal enteropeptidase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Hyperammonaemia, type III |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| 3-Oxo-5 alpha-steroid delta 4-dehydrogenase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Acid phosphatase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Dihydropteridine reductase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Sphingomyelin/cholesterol lipidosis |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Cutis laxa, autosomal recessive |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Glutamate formiminotransferase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Moderate steroid 21-hydroxylase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|