X-linked muscular dystrophy not predominantly limb girdle 240071003
SNOMED CT code
| SNOMED code | 240071003 |
|---|---|
| name | X-linked muscular dystrophy not predominantly limb girdle |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | X-linked muscular dystrophy not predominantly limb girdle (disorder) |
| synonyms | X-linked muscular dystrophy not predominantly limb girdle |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Dystrophy 4720007 |
| Finding site | Skeletal muscle structure 127954009 |
| attributes - group2 | |
| Clinical course | Progressive 255314001 |
| parents | |
| children | Benign scapuloperoneal muscular dystrophy with cardiomyopathy 240072005 removed: 2021-07-31 |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Muscle finding 106030000 Disorder of muscle 129565002 Disorder of skeletal muscle 75047002 Congenital anomaly of skeletal muscle 89886004 Congenital hereditary muscular dystrophy 111501005 X-linked muscular dystrophy not predominantly limb girdle 240071003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Sex-linked hereditary disorder 82852009 X-linked hereditary disease 128430005 X-linked muscular dystrophy not predominantly limb girdle 240071003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Muscular dystrophy 73297009 Muscular dystrophy not predominantly limb girdle in distribution 240070002 X-linked muscular dystrophy not predominantly limb girdle 240071003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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