Taurodontia with absent teeth and sparse hair syndrome 719945007
SNOMED CT code
| SNOMED code | 719945007 |
|---|---|
| name | Taurodontia with absent teeth and sparse hair syndrome |
| status | active |
| date introduced | 2017-01-31 |
| fully specified name(s) | Taurodontia with absent teeth and sparse hair syndrome (disorder) |
| synonyms | Taurodontia with absent teeth and sparse hair syndrome |
| attributes - group1 | |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Finding site | Dentition 245543004 |
| Associated morphology | Absence 418560003 |
| attributes - group2 | |
| Finding site | Ectoderm structure 63206006 |
| Pathological process | Pathological developmental process 308490002 |
| Occurrence | Congenital 255399007 |
| Associated morphology | Dysplasia 25723000 |
| attributes - group3 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Finding site | Hair structure 386045008 |
| attributes - group4 | |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Tooth structure 38199008 |
| Associated morphology | Congenital abnormal number 61295008 |
| Occurrence | Congenital 255399007 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Disorder of tooth development 371136004 Malformation of tooth 422775003 Malformation of teeth 1162865004 Taurodontia with absent teeth and sparse hair syndrome 719945007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Developmental absence of tooth 234951001 Taurodontia with absent teeth and sparse hair syndrome 719945007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of embryonic structure 609521009 Congenital ectodermal defect 254154003 Ectodermal dysplasia 8654005 Ectodermal dysplasia with hair-tooth defects 239027006 Taurodontia with absent teeth and sparse hair syndrome 719945007 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Taurodontia with absent teeth and sparse hair syndrome 719945007 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Finding of mouth region 423066003 Oral cavity finding 116337000 Congenital abnormality of oral cavity 282041002 Congenital anomaly of tooth 422977003 Congenital anomaly in number of teeth 410066003 Partial congenital absence of teeth 64969001 Taurodontia with absent teeth and sparse hair syndrome 719945007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Taurodontia with absent teeth and sparse hair syndrome 719945007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Taurodontia with absent teeth and sparse hair syndrome 719945007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disorder of jaw 37156001 Congenital anomaly of jaw 95473006 Congenital absence of jaw 91922000 Taurodontia with absent teeth and sparse hair syndrome 719945007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disease of mouth 118938008 Congenital anomaly of mouth 128334002 Congenital absence of mouth 91946007 Taurodontia with absent teeth and sparse hair syndrome 719945007 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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