Rothmund Thomson syndrome type 2 1003923009
SNOMED CT code
SNOMED code | 1003923009 |
---|---|
name | Rothmund Thomson syndrome type 2 |
status | active |
date introduced | 2021-01-31 |
fully specified name(s) | Rothmund Thomson syndrome type 2 (disorder) |
synonyms | Rothmund Thomson syndrome type 2 |
attributes - group1 | |
Finding site | Skin structure 39937001 |
Associated morphology | Poikiloderma 70114006 |
Occurrence | Congenital 255399007 |
Pathological process | Pathological developmental process 308490002 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Rothmund-Thomson syndrome 69093006 Rothmund Thomson syndrome type 2 1003923009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Rothmund Thomson syndrome type 2 1003923009 |
ancestors | sorted most to least specific
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cpt crosswalks |
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