Neuroectodermal melanolysosomal disease 724091002
SNOMED CT code
| SNOMED code | 724091002 |
|---|---|
| name | Neuroectodermal melanolysosomal disease |
| status | active |
| date introduced | 2017-07-31 |
| fully specified name(s) | Neuroectodermal melanolysosomal disease (disorder) |
| synonyms |
|
| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Skin structure 39937001 |
| Associated morphology | Hyperpigmentation 4830009 |
| attributes - group2 | |
| Pathological process | Pathological developmental process 308490002 |
| Associated morphology | Morphologically abnormal structure 49755003 |
| Occurrence | Congenital 255399007 |
| Finding site | Nervous system structure 25087005 |
| attributes - group3 | |
| Finding site | Nervous system structure 25087005 |
| Associated morphology | Neoplasm 108369006 |
| Occurrence | Congenital 255399007 |
| attributes - group4 | |
| Associated morphology | Neoplasm 108369006 |
| Occurrence | Congenital 255399007 |
| Finding site | Skin structure 39937001 |
| parents |
|
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Congenital pigmentary skin anomalies 205564003 Neuroectodermal melanolysosomal disease 724091002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Neuroectodermal melanolysosomal disease 724091002 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Neuroectodermal melanolysosomal disease 724091002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Hereditary disorder of nervous system 363235000 Neuroectodermal melanolysosomal disease 724091002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Hyperpigmentation of skin 49765009 Neuroectodermal melanolysosomal disease 724091002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic disorder of skin pigmentation 724839001 Neuroectodermal melanolysosomal disease 724091002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Congenital disease 66091009 Neurocutaneous syndrome 78572006 Neuroectodermal melanolysosomal disease 724091002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Congenital malformation 276654001 Congenital malformation syndrome 400038003 Multiple system malformation syndrome 82354003 Neuroectodermal melanolysosomal disease 724091002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Neuroectodermal melanolysosomal disease 724091002 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Disorder of body system 362965005 Disorder of nervous system 118940003 Congenital anomaly of nervous system 88425004 Neuroectodermal melanolysosomal disease 724091002 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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