Oculocerebral hypopigmentation syndrome of Preus type 716174001
SNOMED CT code
| SNOMED code | 716174001 |
|---|---|
| name | Oculocerebral hypopigmentation syndrome of Preus type |
| status | active |
| date introduced | 2016-07-31 |
| fully specified name(s) | Oculocerebral hypopigmentation syndrome of Preus type (disorder) |
| synonyms |
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| attributes - group1 | |
| Occurrence | Congenital 255399007 |
| Pathological process | Pathological developmental process 308490002 |
| Finding site | Hair structure 386045008 |
| Associated morphology | Hypopigmentation 89031001 |
| parents | |
| hierarchies | a selection of possible paths SNOMED CT Concept 138875005Clinical finding 404684003 Disease 64572001 Disorder of pigmentation 414032001 Disorder of skin pigmentation 46690002 Skin hypopigmented 23006000 Congenital deficiency of pigment of skin 1953005 Oculocerebral hypopigmentation syndrome of Preus type 716174001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Developmental disorder 5294002 Developmental hereditary disorder 363070008 Oculocerebral hypopigmentation syndrome of Preus type 716174001 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Hereditary disorder of the integument 363185004 Oculocerebral hypopigmentation syndrome of Preus type 716174001 SNOMED CT Concept 138875005 Clinical finding 404684003 Integumentary system finding 106077005 Disorder of integument 128598002 Congenital anomaly of integument 38164009 Congenital anomaly of skin 199879009 Congenital anomaly of hair 65033000 Oculocerebral hypopigmentation syndrome of Preus type 716174001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Genetic disorder of skin pigmentation 724839001 Oculocerebral hypopigmentation syndrome of Preus type 716174001 SNOMED CT Concept 138875005 Clinical finding 404684003 Disease 64572001 Genetic disease 782964007 Hereditary disease 32895009 Autosomal hereditary disorder 1899006 Autosomal recessive hereditary disorder 85995004 Oculocerebral hypopigmentation syndrome of Preus type 716174001 |
| ancestors | sorted most to least specific
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| cpt crosswalks | |
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