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ili-30-14160365-n CILI: i111320
WordNet Domains: medicine
SUMO Ontology: DiseaseOrSyndrome+
Basic Level Concept: 14070360-n disease
Epinonyms: [1] congenital_disease
[1] congenital_disease |1|
[0] ili-30-14160365-n (has_hyperonym) |1|
Polarity:
  positive negative
SentiWordNet: 0.125 0.5
ML-SentiCon: 0.125 0.25
Time:
  past present future atemporal
TempoWordNet: 0 0 0 1

Explore the terminological domain with [Termonet]
GL Variants
- especializado distrofia_muscular · [RILG] [DRAG]
CA Variants
- distròfia_muscular
Gloss
Transtorn patològic que es caracteritza per la pèrdua de les capacitats funcionals d'un òrgan o teixit i que afecta la nutrició i el creixement
EU Variants
- distrofia
ES Variants
- distrofia
- distrofia_muscular
EN Variants
- dystrophy ['dɪstrəfi]
- muscular_dystrophy
Gloss
any of several hereditary diseases of the muscular system characterized by weakness and wasting of skeletal muscles
DE Variants
- Dystrophie
- Muskeldystrophie
IT Variants
- distrofia muscolare
FR Variants
- dystrophie
- dystrophie_musculaire
- myopathie_de_Duchenne
- myopathie_de_duchenne
ZH_S Variants
- 肌肉萎缩症
- 营养失调
Lexical relations in WordNet via ILI (18) - Show / Hide graph:
Hyperonyms
(has_hyperonym)
14151139-n: a disease or disorder that is inherited genetically
Hyponyms
(has_hyponym)
14161075-n: a form of muscular dystrophy that sets in in adolescence or adulthood and progresses slowly but will affect all voluntary muscles; characterized by generalized weakness and muscle wasting that affects limb and trunk muscles first; similar to Duchenne's muscular dystrophy but less severe; inheritance is X-linked recessive (carried by females but affecting only males)
Hyponyms
(has_hyponym)
14161515-n: a form of muscular dystrophy that sets in between 40 and 60 years of age and is characterized by weakness and wasting of the muscles of the hands and forearms and lower legs; inheritance is autosomal dominant
Hyponyms
(has_hyponym)
14161795-n: the most common form of muscular dystrophy; inheritance is X-linked recessive (carried by females but affecting only males)
Hyponyms
(has_hyponym)
14162563-n: an autosomal recessive form of muscular dystrophy that appears anywhere from late childhood to middle age; characterized by progressive muscular weakness beginning either in the shoulder or pelvic girdle; usually progresses slowly with cardiopulmonary complications in the later stages
Hyponyms
(has_hyponym)
14163182-n: a severe form of muscular dystrophy marked by generalized weakness and muscular wasting that affects the face and feet and hands and neck; difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips; the onset can be any time from birth to middle age and the progression is slow; inheritance is autosomal dominant
Hyponyms
(has_hyponym)
14163676-n: a form of muscular dystrophy that usually begins between early adulthood and middle age and first affects muscles of the eyelid and throat; progresses slowly with swallowing problems common as the disease progresses; inheritance is autosomal dominant
Glosses
(gloss)
02882570-a: of or relating to or consisting of muscle
Glosses
(gloss)
05040275-n: the property of lacking physical or mental strength; liability to failure under pressure or stress or strain
Glosses
(gloss)
05289861-n: a muscle that is connected at either or both ends to a bone and so move parts of the skeleton; a muscle that is characterized by transverse stripes
Glosses
(gloss)
14151139-n: a disease or disorder that is inherited genetically
Glosses
(gloss)
14365741-n: a decrease in size of an organ caused by disease or disuse
Glosses
(rgloss)
14161075-n: a form of muscular dystrophy that sets in in adolescence or adulthood and progresses slowly but will affect all voluntary muscles; characterized by generalized weakness and muscle wasting that affects limb and trunk muscles first; similar to Duchenne's muscular dystrophy but less severe; inheritance is X-linked recessive (carried by females but affecting only males)
Glosses
(rgloss)
14161515-n: a form of muscular dystrophy that sets in between 40 and 60 years of age and is characterized by weakness and wasting of the muscles of the hands and forearms and lower legs; inheritance is autosomal dominant
Glosses
(rgloss)
14161795-n: the most common form of muscular dystrophy; inheritance is X-linked recessive (carried by females but affecting only males)
Glosses
(rgloss)
14162563-n: an autosomal recessive form of muscular dystrophy that appears anywhere from late childhood to middle age; characterized by progressive muscular weakness beginning either in the shoulder or pelvic girdle; usually progresses slowly with cardiopulmonary complications in the later stages
Glosses
(rgloss)
14163182-n: a severe form of muscular dystrophy marked by generalized weakness and muscular wasting that affects the face and feet and hands and neck; difficult speech and difficulty with the hands that spreads to the arms and shoulders and legs and hips; the onset can be any time from birth to middle age and the progression is slow; inheritance is autosomal dominant
Glosses
(rgloss)
14163676-n: a form of muscular dystrophy that usually begins between early adulthood and middle age and first affects muscles of the eyelid and throat; progresses slowly with swallowing problems common as the disease progresses; inheritance is autosomal dominant