n14155834
| type | n |
| lex_filenum | 26 |
| def | any of a number of diseases in which an inherited defect (usually a missing or inadequate enzyme) results in an abnormality of metabolism |
| Outgoing links | |
| Hypernym | metabolic disorder; genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition |
| Hyponym | galactosemia; lysinemia; Niemann-Pick disease; phenylketonuria, PKU |
| Incoming links | |
| Hyponym | metabolic disorder; genetic disease, genetic disorder, genetic abnormality, genetic defect, congenital disease, inherited disease, inherited disorder, hereditary disease, hereditary condition |
| Hypernym | galactosemia; lysinemia; Niemann-Pick disease; phenylketonuria, PKU |
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