Galnet - Galician WordNet 3.0

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Search variants in 
ili-30-03145310-a CILI: i18085
WordNet Domains:
SUMO Ontology:
Top Ontology:
Basic Level Concept:
Epinonyms: [3] genetics
[3] genetics |0.93|
[2] ili-30-05443651-n (category) |0.95|
[1] ili-30-05442594-n (has_hyperonym) |1|
[0] ili-30-03145310-a (pertains_to) |0.85|
Polarity:
  positive negative
SentiWordNet: 0 0
ML-SentiCon: 0 0
Time:
  past present future atemporal
TempoWordNet: 0 0.001202 0.599798 0.399

Explore the terminological domain with [Termonet]
EN Variants
- X-linked
an X-linked mutation
Gloss
relating to genes or characteristics or conditions carried on the X chromosome
ZH_S Variants
- X染色体+的
- 链表
Lexical relations in WordNet via ILI (10) - Show / Hide graph:
Related
(pertains_to)
05442594-n: the sex chromosome that is present in both sexes: singly in males and doubly in females
Glosses
(gloss)
02079933-v: transmit or serve as the medium for transmission
Glosses
(gloss)
02676054-v: be relevant to
Glosses
(gloss)
04731497-n: a distinguishing quality
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)
05442594-n: the sex chromosome that is present in both sexes: singly in males and doubly in females
Glosses
(gloss)
05849789-n: a prominent attribute or aspect of something
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)
14161795-n: the most common form of muscular dystrophy; inheritance is X-linked recessive (carried by females but affecting only males)
Glosses
(rgloss)
14208587-n: a form of neuropathy that can begin between childhood and young adulthood; characterized by weakness and atrophy of the muscles of the hands and lower legs; progression is slow and individuals affected can have a normal life span; inheritance is X-linked recessive or X-linked dominant