Amelogenesis imperfecta, pigmented hypomaturation type 109474009
SNOMED CT code
| SNOMED code | 109474009 |
|---|---|
| name | Amelogenesis imperfecta, pigmented hypomaturation type |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Amelogenesis imperfecta, pigmented hypomaturation type (disorder) |
| synonyms | Amelogenesis imperfecta, pigmented hypomaturation type |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Enamel structure 76993005 |
| Associated morphology | Pigment deposition 51083003 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disease of mouth 118938008 Oral lesion 1071000119107 Amelogenesis imperfecta, pigmented hypomaturation type 109474009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Amelogenesis imperfecta 78494001 Amelogenesis imperfecta, hypomaturation type 109475005 Amelogenesis imperfecta, pigmented hypomaturation type 109474009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Amelogenesis imperfecta, pigmented hypomaturation type 109474009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Amelogenesis imperfecta, pigmented hypomaturation type 109474009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Amelogenesis imperfecta, pigmented hypomaturation type 109474009 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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