Alstrom syndrome 63702009
SNOMED CT code
| SNOMED code | 63702009 |
|---|---|
| name | Alstrom syndrome |
| status | active |
| date introduced | 2002-01-31 |
| fully specified name(s) | Alstrom syndrome (disorder) |
| synonyms | Alstrom syndrome |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| attributes - group3 | |
| Has interpretation | Above reference range 281302008 |
| Interprets | Body weight measure 363808001 |
| attributes - group6 | |
| Finding site | Endocrine pancreatic structure 78696007 |
| attributes - group4 | |
| Has interpretation | Decreased 1250004 |
| Interprets | Hearing 47078008 |
| attributes - group1 | |
| Finding site | Retinal structure 5665001 |
| Associated morphology | Dystrophy 4720007 |
| attributes - group5 | |
| Finding site | Auditory structure 91159003 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Decreased hearing 103276001 Alstrom syndrome 63702009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Hereditary metabolic disease 1821000146108 Alstrom syndrome 63702009 SNOMED CT Concept 138875005 Clinical finding 404684003 Ear and auditory finding 118236001 Disorder of auditory system 362966006 Auditory system hereditary disorder 362991006 Alstrom syndrome 63702009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Alstrom syndrome 63702009 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 Alstrom syndrome 63702009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Hereditary disorder of endocrine system 363104002 Alstrom syndrome 63702009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Obesity 414916001 Alstrom syndrome 63702009 SNOMED CT Concept 138875005 Clinical finding 404684003 Eye / vision finding 118235002 Visual system disorder 128127008 Hereditary disorder of the visual system 363343008 Hereditary retinal dystrophy 41799005 Alstrom syndrome 63702009 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Hearing finding 118230007 Hearing disorder 128540005 Hearing loss 15188001 Sensorineural hearing loss 60700002 Alstrom syndrome 63702009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of endocrine system 362969004 Insulin resistance 763325000 Alstrom syndrome 63702009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Alstrom syndrome 63702009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of carbohydrate metabolism 20957000 Disorder of glucose regulation 237597000 Hyperinsulinism 83469008 Alstrom syndrome 63702009 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Alstrom syndrome 63702009 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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