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 |
|