Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome 733028000
SNOMED CT code
| SNOMED code | 733028000 |
|---|---|
| name | Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome (disorder) |
| synonyms | Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Associated morphology | Demyelination 32693004 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Central nervous system structure 21483005 |
| attributes - group2 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Proliferative hyperkeratosis 773635001 |
| Finding site | Entire skin 181469002 |
| attributes - group3 | |
| Has interpretation | Abnormal 263654008 |
| Interprets | Hemostatic function 74848003 |
| attributes - group4 | |
| Has interpretation | Abnormal 263654008 |
| Interprets | Keratinization 44138005 |
| attributes - group6 | |
| Pathological process | Abnormal immune process 769247005 |
| Associated morphology | Inflammatory morphology 409774005 |
| Finding site | Central nervous system structure 21483005 |
| attributes - group5 | |
| Pathological process | Abnormal immune process 769247005 |
| Associated morphology | Demyelination 32693004 |
| Finding site | Central nervous system structure 21483005 |
| parents |
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| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Degenerative disease of the central nervous system 80690008 Hereditary degenerative disease of central nervous system 106018006 Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome 733028000 SNOMED CT Concept 138875005 Clinical finding 404684003 Central nervous system finding 246556002 Disorder of the central nervous system 23853001 Congenital anomaly of central nervous system 128124001 Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome 733028000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Hereditary coagulation factor deficiency 16922007 Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome 733028000 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Skin finding 106076001 Rough skin 816995008 Congenital ichthyosis of skin 13059002 Lamellar ichthyosis 205550003 Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome 733028000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Multiple sclerosis 24700007 Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome 733028000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of immune function 414029004 Hereditary disorder of immune system 363138005 Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome 733028000 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Degenerative disorder 362975008 Congenital degeneration of nervous system 95477007 Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome 733028000 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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