Tyrosinase-positive oculocutaneous albinism 26336006

SNOMED CT code

SNOMED code

26336006

name

Tyrosinase-positive oculocutaneous albinism

status

active

date introduced

2002-01-31

fully specified name(s)

Tyrosinase-positive oculocutaneous albinism (disorder)

synonyms

OCA2 - Tyrosinase-positive oculocutaneous albinism
Albinoidism
Oculocutaneous albinism type 2
Tyrosinase-positive oculocutaneous albinism

attributes - group2

Finding site

Eye structure 81745001

Pathological process

Pathological developmental process 308490002

Occurrence

Congenital 255399007

Associated morphology

Decreased melanin pigmentation 37257004

attributes - group1

Pathological process

Pathological developmental process 308490002

Finding site

Skin structure 39937001

Associated morphology

Decreased melanin pigmentation 37257004

Occurrence

Congenital 255399007

parents

Oculocutaneous albinism 63844009

children

Brown oculocutaneous albinism 11160000
Hermansky-Pudlak syndrome 9311003
Punctate oculocutaneous albinoidism 62144003
Rufous albinism 63450009

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Integumentary system finding 106077005
Disorder of integument 128598002
Hereditary disorder of the integument 363185004
Oculocutaneous albinism 63844009
Tyrosinase-positive oculocutaneous albinism 26336006

ancestors

sorted most to least specific

Oculocutaneous albinism 63844009
Albinism 15890002
Hereditary disorder of the integument 363185004
Hereditary disorder of the visual system 363343008
Congenital oculocutaneous hypopigmentation 61649007
Genetic disorder of skin pigmentation 724839001
Autosomal recessive hereditary disorder 85995004
Congenital anomaly of eye 19416009
Autosomal hereditary disorder 1899006
Developmental hereditary disorder 363070008
Inborn error of metabolism 86095007
Hereditary disorder by system 363137000
Congenital deficiency of pigment of skin 1953005
Lesion of eye 301905003
Anomaly of eye 11131000119108
Hereditary metabolic disease 1821000146108
Congenital pigmentary skin anomalies 205564003
Congenital anomaly of visual system 127329003
Congenital anomaly of head 87290003
Skin hypopigmented 23006000
Disorder of eye 371405004
Disorder of skin pigmentation 46690002
Hereditary disease 32895009
Congenital anomaly of skin 199879009
Metabolic disease 75934005
Disorder of sensory organ 1279550006
Disorder of pigmentation 414032001
Genetic disease 782964007
Congenital anomaly of integument 38164009
Globe finding 246915008
Disorder of eye region 371409005
Skin lesion 95324001
Congenital malformation 276654001
Visual system disorder 128127008
Disorder of head 118934005
Soft tissue lesion 239953001
Disorder of skin 95320005
Finding of head region 298364001
Lesion of skin and/or skin-associated mucous membrane 714974000
Developmental disorder 5294002
Eye / vision finding 118235002
Congenital disease 66091009
Head finding 406122000
Skin finding 106076001
Skin or mucosa lesion 247440002
Disorder of skin and/or subcutaneous tissue 80659006
Disorder of integument 128598002
Finding of head and neck region 118254002
Disorder of soft tissue 19660004
Skin AND/OR mucosa finding 415531008
Integumentary system finding 106077005
Disorder of body system 362965005
General finding of soft tissue 248402002
Disease 64572001
Clinical finding 404684003
SNOMED CT Concept 138875005

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SNOMED CT Concept 138875005

Clinical finding 404684003

Integumentary system finding 106077005

Disorder of integument 128598002

Hereditary disorder of the integument 363185004

Oculocutaneous albinism 63844009

Tyrosinase-positive oculocutaneous albinism 26336006

SNOMED CT code