Trichothiodystrophy 723551003
SNOMED CT code
| SNOMED code | 723551003 |
|---|---|
| name | Trichothiodystrophy |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Trichothiodystrophy (disorder) |
| synonyms | Trichothiodystrophy |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Hair shaft structure 37111008 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Ectoderm structure 63206006 |
| Associated morphology | Dysplasia 25723000 |
| parents | |
| children |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Trichothiodystrophy 723551003 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Trichothiodystrophy 723551003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic defect of hair shaft 402774006 Trichothiodystrophy 723551003 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 Trichothiodystrophy 723551003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Trichothiodystrophy 723551003 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Congenital ectodermal defect 254154003 Ectodermal dysplasia 8654005 Trichothiodystrophy 723551003 |
| ancestors | sorted most to least specific
|
| cpt crosswalks | |
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