Piebald trait with neurologic defects syndrome 773984007
SNOMED CT code
SNOMED code | 773984007 |
---|---|
name | Piebald trait with neurologic defects syndrome |
status | active |
date introduced | 2019-01-31 |
fully specified name(s) | Piebald trait with neurologic defects syndrome (disorder) |
synonyms |
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attributes - group1 | |
Pathological process | Pathological developmental process 308490002 |
Occurrence | Congenital 255399007 |
Finding site | Skin structure 39937001 |
Associated morphology | Hypopigmentation 89031001 |
attributes - group2 | |
Interprets | Intellectual ability 247573007 |
Has interpretation | Impaired 260379002 |
attributes - group3 | |
Interprets | Adaptation behavior 406208005 |
Has interpretation | Impaired 260379002 |
parents | |
hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Mental state, behavior and/or psychosocial function finding 384821006 Behavior finding 844005 Intellectual disability 110359009 Piebald trait with neurologic defects syndrome 773984007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal dominant hereditary disorder 11164009 Piebald trait with neurologic defects syndrome 773984007 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 Piebald trait with neurologic defects syndrome 773984007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Piebald trait with neurologic defects syndrome 773984007 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Piebald trait with neurologic defects syndrome 773984007 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic disorder of skin pigmentation 724839001 Piebald trait with neurologic defects syndrome 773984007 |
ancestors | sorted most to least specific
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cpt crosswalks |
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