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loading...| Preferred Name |
sÃndrome del cromosoma X frágil |
|
| Synonyms |
sÃndrome del cromosoma X frágil (trastorno) sÃndrome de Martin - Bell |
|
| ID |
http://purl.bioontology.org/ontology/SCTSPA/613003 |
|
| Active |
1 |
|
| altLabel |
sÃndrome del cromosoma X frágil (trastorno) sÃndrome de Martin - Bell |
|
| Associated finding of | ||
| CASE SIGNIFICANCE ID |
900000000000017005 |
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| Cause of | ||
| cui |
C0016667 |
|
| DEFINITION STATUS ID |
900000000000074008 |
|
| Effective time |
20020131 |
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| Has associated morphology | ||
| Has finding site | ||
| Has interpretation | ||
| Has pathological process | ||
| interprets | ||
| Module ID |
450829007 |
|
| notation |
613003 |
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| Occurs in | ||
| prefLabel |
sÃndrome del cromosoma X frágil |
|
| Subset member |
450828004~ACCEPTABILITYID~900000000000549004 450828004~ACCEPTABILITYID~900000000000548007 |
|
| tui |
T047 |
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| Type ID |
900000000000003001 900000000000013009 |
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| subClassOf |
http://purl.bioontology.org/ontology/SCTSPA/363070008 http://purl.bioontology.org/ontology/SCTSPA/110359009 http://purl.bioontology.org/ontology/SCTSPA/205720009 |
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