Autosomal dominant palmoplantar keratoderma and congenital alopecia 719518004
SNOMED CT code
| SNOMED code | 719518004 |
|---|---|
| name | Autosomal dominant palmoplantar keratoderma and congenital alopecia |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Autosomal dominant palmoplantar keratoderma and congenital alopecia (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Hair structure 386045008 |
| Associated morphology | Absence 418560003 |
| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Ectoderm structure 63206006 |
| Associated morphology | Dysplasia 25723000 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Hyperkeratosis 26996000 |
| Finding site | Skin structure 39937001 |
| attributes - group4 | |
| Finding site | Skin structure of sole of foot 37136002 |
| Associated morphology | Hyperkeratosis 26996000 |
| attributes - group5 | |
| Associated morphology | Hyperkeratosis 26996000 |
| Finding site | Skin structure of palmar area of hand 70887009 |
| 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 Autosomal dominant palmoplantar keratoderma and congenital alopecia 719518004 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Hereditary palmoplantar keratoderma 239066003 Autosomal dominant palmoplantar keratoderma and congenital alopecia 719518004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Congenital ectodermal defect 254154003 Autosomal dominant palmoplantar keratoderma and congenital alopecia 719518004 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 Congenital anomaly of hair 65033000 Congenital alopecia 2965006 Autosomal dominant palmoplantar keratoderma and congenital alopecia 719518004 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Autosomal dominant palmoplantar keratoderma and congenital alopecia 719518004 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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