Isolated congenital adermatoglyphia 763748007
SNOMED CT code
SNOMED code | 763748007 |
---|---|
name | Isolated congenital adermatoglyphia |
status | active |
date introduced | 2018-07-31 |
fully specified name(s) | Isolated congenital adermatoglyphia (disorder) |
synonyms |
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attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Associated morphology | Absence 418560003 |
Occurrence | Congenital 255399007 |
Finding site | Entire dermatoglyphic patterns 314292007 |
parents | |
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 Isolated congenital adermatoglyphia 763748007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Isolated congenital adermatoglyphia 763748007 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Isolated congenital adermatoglyphia 763748007 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Abnormal dermatoglyphic pattern 83145004 Isolated congenital adermatoglyphia 763748007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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