HELIX syndrome 1217380005
SNOMED CT code
| SNOMED code | 1217380005 |
|---|---|
| name | HELIX syndrome |
| status | active |
| date introduced | 2022-04-30 |
| fully specified name(s) | Hypohidrosis, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, xerostomia syndrome (disorder) |
| synonyms |
|
| attributes - group5 | |
| Finding site | Sweat gland structure 10410005 |
| attributes - group6 | |
| Finding site | Salivary gland structure 385294005 |
| attributes - group7 | |
| Finding site | Renal tubule structure 58471003 |
| attributes - group3 | |
| Interprets | Sweating 415691001 |
| Has interpretation | Decreased 1250004 |
| attributes - group4 | |
| Interprets | Tear production 64702000 |
| Has interpretation | Decreased 1250004 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Finding site | Lacrimal gland structure 13561001 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Pathological process | Pathological developmental process 308490002 |
| attributes - group1 | |
| Finding site | Entire skin 181469002 |
| Associated morphology | Hyperkeratosis 26996000 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Disorder of fluid AND/OR electrolyte 76314005 Disorder of electrolytes 237840007 Electrolyte imbalance 105593004 HELIX syndrome 1217380005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Metabolic disease 75934005 Metabolic renal disease 106000008 HELIX syndrome 1217380005 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Decline in functional status 154091000119106 Alacrima 253215004 HELIX syndrome 1217380005 SNOMED CT Concept 138875005 Clinical finding 404684003 Digestive system finding 386617003 Disorder of digestive system 53619000 Digestive system hereditary disorder 363080007 HELIX syndrome 1217380005 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 HELIX syndrome 1217380005 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Hereditary nephropathy 367591000119105 HELIX syndrome 1217380005 SNOMED CT Concept 138875005 Clinical finding 404684003 Functional finding 118228005 Decline in functional status 154091000119106 Hypohidrosis 45004005 HELIX syndrome 1217380005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Keratosis 254666005 Keratoderma 707209001 Ichthyosis 782957005 HELIX syndrome 1217380005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 HELIX syndrome 1217380005 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of head 118934005 Disease of mouth 118938008 Disorder of salivary structure 283015002 Disorder of salivary gland 10890000 Disturbance of salivary secretion 78948009 Xerostomia 87715008 HELIX syndrome 1217380005 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Salt-losing nephropathy 91003006 HELIX syndrome 1217380005 SNOMED CT Concept 138875005 Clinical finding 404684003 Viscus structure finding 406123005 Abdominal organ finding 249561001 Kidney finding 249578005 Kidney disease 90708001 Disorder of renal parenchyma 767094002 Renal tubular disorder 95568003 HELIX syndrome 1217380005 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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