Autosomal dominant aplasia and myelodysplasia 778006008
SNOMED CT code
| SNOMED code | 778006008 |
|---|---|
| name | Autosomal dominant aplasia and myelodysplasia |
| status | active |
| date introduced | 2019-01-31 |
| fully specified name(s) | Autosomal dominant aplasia and myelodysplasia (disorder) |
| synonyms |
|
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Inner ear structure 22945000 |
| attributes - group1 | |
| Finding site | Bone marrow structure 14016003 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Interprets | Hearing 47078008 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital anomaly of ear with impairment of hearing 111339003 Autosomal dominant aplasia and myelodysplasia 778006008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Autosomal dominant aplasia and myelodysplasia 778006008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of hematopoietic structure 414027002 Bone marrow disorder 127035006 Autosomal dominant aplasia and myelodysplasia 778006008 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Autosomal dominant aplasia and myelodysplasia 778006008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Autosomal dominant aplasia and myelodysplasia 778006008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of ear 25906001 Disorder of inner ear 232297009 Congenital anomaly of inner ear 43353004 Autosomal dominant aplasia and myelodysplasia 778006008 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital deafness 95828007 Autosomal dominant aplasia and myelodysplasia 778006008 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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