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ili-30-14074877-n CILI: i110895
WordNet Domains: medicine
SUMO Ontology: DiseaseOrSyndrome+
Basic Level Concept: 14070360-n disease
Epinonyms: [1] congenital_disease
[1] congenital_disease |1|
[0] ili-30-14074877-n (has_hyperonym) |1|
Polaridade:
  positivo negativo
SentiWordNet: 0 0
ML-SentiCon: 0 0.25
Tempo:
  pasado presente futuro atemporal
TempoWordNet: 0 0 0 1

Explorar o ámbito terminolóxico en [Termonet]
GL Variantes
- desorde_monoxénica · [RILG] [DRAG]
- enfermidade_monoxénica · [RILG] [DRAG]
EN Variantes
- monogenic_disease
- monogenic_disorder
Glosa
an inherited disease controlled by a single pair of genes
ZH_S Variantes
- 遗传病
Relacións léxico-semánticas no WordNet vía ILI (13) - Amosar / Agochar gráfico:
Hyperonyms
(has_hyperonym)
14151139-n: a disease or disorder that is inherited genetically
Hyponyms
(has_hyponym)
14128812-n: a congenital disease affecting T cells that can result from a mutation in any one of several different genes; children with it are susceptible to infectious disease; if untreated it is lethal within the first year or two of life
Hyponyms
(has_hyponym)
14155506-n: the most common congenital disease; the child's lungs and intestines and pancreas become clogged with thick mucus; caused by defect in a single gene; no cure is known
Hyponyms
(has_hyponym)
14156345-n: a rare chronic disorder of lipid metabolism of genetic origin
Hyponyms
(has_hyponym)
14156976-n: hereditary disease; develops in adulthood and ends in dementia
Hyponyms
(has_hyponym)
14157163-n: hereditary disease (autosomal recessive) consisting of an error is mucopolysaccharide metabolism; characterized by severe abnormalities in development of skeletal cartilage and bone and mental retardation
Hyponyms
(has_hyponym)
14158179-n: autosomal dominant disease characterized by numerous neurofibromas and by spots on the skin and often by developmental abnormalities
Hyponyms
(has_hyponym)
14168792-n: a congenital form of anemia occurring mostly in blacks; characterized by abnormal blood cells having a crescent shape
Hyponyms
(has_hyponym)
14169364-n: a hereditary disorder of lipid metabolism occurring most frequently in individuals of Jewish descent in eastern Europe; accumulation of lipids in nervous tissue results in death in early childhood
Hyponyms
(has_hyponym)
14195715-n: an inherited form of anemia caused by faulty synthesis of hemoglobin
Hyponyms
(has_hyponym)
14466974-n: congenital disorder characterized by high levels of cholesterol and early development of atherosclerosis
Glosses
(gloss)
05436752-n: (genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity
Glosses
(gloss)
14151139-n: a disease or disorder that is inherited genetically