| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Ateliotic dwarfism without insulinopenia |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Kerasin thesaurismosis (disorder) |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Galactosylceramide lipidosis |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Westphal-Strumpell syndrome |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Wilson's disease * |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Testicular tumor of adrenogenital syndrome |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Craniodiaphyseal dysplasia |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Congenital pancreatic enterokinase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Mandibuloacral dysostosis |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Testicular tumor of adrenogenital syndrome |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Laurence-Moon syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Tay-Sachs disease |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Acatalasia |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Fukuyama congenital muscular dystrophy |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Walker-Warburg congenital muscular dystrophy |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Muscle-eye-brain disease, congenital muscular dystrophy |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| HNSHA due to glutathione synthetase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Hereditary methemoglobinemia, 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 |
|
| Methylcrotonyl-CoA carboxylase deficiency |
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-coenzyme A-carboxylase) ligase deficiency |
Is a |
False |
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 fructosuria |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Beta-aminoisobutyric aciduria (disorder) |
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 |
|
| 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 |
|
| 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-biphosphatase 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 |
|
| 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 |
|
| 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 |
|
| Orotic aciduria |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Hypervalinemia |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Corticosterone 18-monooxygenase deficiency |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Hypertyrosinemia, Richner-Hanhart type (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Phosphatidylcholine-sterol acyltransferase deficiency |
Is a |
False |
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 |
|
| Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency (disorder) |
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 |
|
| 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 |
|
| Hyperammonemia, 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 |
|
| Purine-nucleoside phosphorylase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Urocanate hydratase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Proline dehydrogenase deficiency (disorder) |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Muscle phosphoglycerate mutase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| HNSHA due to diphosphoglycerate mutase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Congenital hyperammonemia, type I |
Is a |
False |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Cholestanol storage disease |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Glycine dehydrogenase (decarboxylating) deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Alstrom syndrome |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|
| Porphobilinogen synthase deficiency |
Is a |
True |
Autosomal recessive hereditary disorder |
Inferred relationship |
Some |
|