Deafness, vitiligo, achalasia syndrome 733069009
SNOMED CT code
| SNOMED code | 733069009 |
|---|---|
| name | Deafness, vitiligo, achalasia syndrome |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Deafness, vitiligo, achalasia syndrome (disorder) |
| synonyms | Deafness, vitiligo, achalasia syndrome |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Cardioesophageal junction structure 25271004 |
| attributes - group2 | |
| Finding site | Inner ear structure 22945000 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Hypopigmentation 89031001 |
| Occurrence | Congenital 255399007 |
| Finding site | Skin structure 39937001 |
| attributes - group5 | |
| Interprets | Hearing 47078008 |
| attributes - group6 | |
| Interprets | Height / growth measure 271603002 |
| attributes - group4 | |
| Has interpretation | Abnormal 263654008 |
| Interprets | Motility 398598008 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital anomaly of ear with impairment of hearing 111339003 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Skin hypopigmented 23006000 Congenital deficiency of pigment of skin 1953005 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Hearing disorder 128540005 Hearing loss 15188001 Hearing loss associated with syndrome 232333009 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Finding of general physiological development 271616002 Disorder of stature 237834000 Short stature disorder 237836003 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of sensory organ 1279550006 Disorder of ear 25906001 Disorder of inner ear 232297009 Congenital anomaly of inner ear 43353004 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Skin hypopigmented 23006000 Vitiligo 56727007 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital achalasia of esophagus 700283004 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic disorder of skin pigmentation 724839001 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Deafness, vitiligo, achalasia syndrome 733069009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Congenital hearing disorder 95827002 Congenital deafness 95828007 Deafness, vitiligo, achalasia syndrome 733069009 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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