n14162275
type | n |
lex_filenum | 26 |
def | a disease caused by the presence of two recessive mutant genes on an autosome |
Outgoing links | |
Hypernym | genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition |
Hyponym | limb-girdle muscular dystrophy; Niemann-Pick disease; Tay-Sachs disease, Tay-Sachs, Sachs disease, infantile amaurotic idiocy; thrombasthenia; tyrosinemia; Werdnig-Hoffman disease |
Incoming links | |
Hyponym | genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition |
Hypernym | limb-girdle muscular dystrophy; Niemann-Pick disease; Tay-Sachs disease, Tay-Sachs, Sachs disease, infantile amaurotic idiocy; thrombasthenia; tyrosinemia; Werdnig-Hoffman disease |
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