Mullerian aplasia 253828000
SNOMED CT code
SNOMED code | 253828000 |
---|---|
name | Mullerian aplasia |
status | active |
date introduced | 2002-01-31 |
fully specified name(s) | Mullerian aplasia (disorder) |
synonyms |
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attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Aplasia 45486003 |
Finding site | Structure of paramesonephric duct 26896004 |
Occurrence | Congenital 255399007 |
parents | |
children | WNT4 Mullerian aplasia and ovarian dysfunction 699275001 |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Mullerian aplasia 253828000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Mullerian aplasia 253828000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Mullerian aplasia 253828000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Mullerian aplasia 253828000 |
ancestors | sorted most to least specific
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cpt crosswalks |
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