monogenic disorder (n)
monogenic disease (n)

n14074877

type n
lex_filenum 26
def an inherited disease controlled by a single pair of genes
Outgoing links
Hypernym genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition
Hyponym severe combined immunodeficiency, severe combined immunodeficiency disease, SCID; cystic fibrosis, CF, fibrocystic disease of the pancreas, pancreatic fibrosis, mucoviscidosis; Gaucher's disease; Huntington's chorea, Huntington's disease; Hurler's syndrome, Hurler's disease, gargoylism, dysostosis multiplex, lipochondrodystrophy; neurofibromatosis, von Recklinghausen's disease; sickle-cell anemia, sickle-cell anaemia, sickle-cell disease, crescent-cell anemia, crescent-cell anaemia, drepanocytic anemia, drepanocytic anaemia; Tay-Sachs disease, Tay-Sachs, Sachs disease, infantile amaurotic idiocy; thalassemia, thalassaemia, Mediterranean anemia, Mediterranean anaemia; familial hypercholesterolemia
Incoming links
Hypernym severe combined immunodeficiency, severe combined immunodeficiency disease, SCID; cystic fibrosis, CF, fibrocystic disease of the pancreas, pancreatic fibrosis, mucoviscidosis; Gaucher's disease; Huntington's chorea, Huntington's disease; Hurler's syndrome, Hurler's disease, gargoylism, dysostosis multiplex, lipochondrodystrophy; neurofibromatosis, von Recklinghausen's disease; sickle-cell anemia, sickle-cell anaemia, sickle-cell disease, crescent-cell anemia, crescent-cell anaemia, drepanocytic anemia, drepanocytic anaemia; Tay-Sachs disease, Tay-Sachs, Sachs disease, infantile amaurotic idiocy; thalassemia, thalassaemia, Mediterranean anemia, Mediterranean anaemia; familial hypercholesterolemia
Hyponym genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition

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