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bn:00021810n
Noun Concept
SYL
No term available
EN
A disease or disorder that is inherited genetically WordNet 3.0
Relations
Sources
IS A
EN
disease
EN
hereditary disorder
HAS KIND
EN
abetalipoproteinemia
EN
achondroplasia
EN
osteopetrosis
EN
autosomal dominant disease
EN
autosomal recessive disease
+348 relations
HAS INSTANCE
Amelia
EN
congenital hyperinsulinism
EN
overgrowth syndrome
EN
hypoalphalipoproteinemia
EN
Partial monosomy 13q
+57 relations
HAS CAUSE
EN
pathology
EN
germline mutation
HEALTH SPECIALTY
EN
medical genetics

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