Congenital oculocutaneous hypopigmentation 61649007

SNOMED CT code

SNOMED code

61649007

name

Congenital oculocutaneous hypopigmentation

status

active

date introduced

2002-01-31

fully specified name(s)

Congenital oculocutaneous hypopigmentation (disorder)

synonyms

Congenital oculocutaneous hypopigmentation

attributes - group1

Occurrence

Congenital 255399007

Pathological process

Pathological developmental process 308490002

Associated morphology

Hypopigmentation 89031001

Finding site

Eye structure 81745001

attributes - group2

Pathological process

Pathological developmental process 308490002

Associated morphology

Hypopigmentation 89031001

Occurrence

Congenital 255399007

Finding site

Skin structure 39937001

parents

Congenital anomaly of eye 19416009
Congenital deficiency of pigment of skin 1953005
Lesion of eye 301905003

children

Oculocutaneous albinism 63844009
Osteoporosis and oculocutaneous hypopigmentation syndrome 722113001
Vici syndrome 719824001
Waardenburg syndrome type 1 1010606009
Waardenburg syndrome type 2 1010636000

hierarchies

a selection of possible paths

SNOMED CT Concept 138875005
Clinical finding 404684003
Eye / vision finding 118235002
Visual system disorder 128127008
Congenital anomaly of visual system 127329003
Congenital anomaly of eye 19416009
Congenital oculocutaneous hypopigmentation 61649007

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
Congenital oculocutaneous hypopigmentation 61649007

SNOMED CT Concept 138875005
Clinical finding 404684003
Disease 64572001
Disorder of sensory organ 1279550006
Disorder of eye 371405004
Anomaly of eye 11131000119108
Lesion of eye 301905003
Congenital oculocutaneous hypopigmentation 61649007

ancestors

sorted most to least specific

Congenital anomaly of eye 19416009
Congenital deficiency of pigment of skin 1953005
Lesion of eye 301905003
Anomaly of eye 11131000119108
Congenital pigmentary skin anomalies 205564003
Congenital anomaly of visual system 127329003
Congenital anomaly of head 87290003
Skin hypopigmented 23006000
Disorder of eye 371405004
Congenital anomaly of skin 199879009
Disorder of skin pigmentation 46690002
Disorder of sensory organ 1279550006
Congenital anomaly of integument 38164009
Globe finding 246915008
Disorder of eye region 371409005
Disorder of pigmentation 414032001
Skin lesion 95324001
Visual system disorder 128127008
Disorder of head 118934005
Disorder of skin 95320005
Congenital malformation 276654001
Finding of head region 298364001
Soft tissue lesion 239953001
Lesion of skin and/or skin-associated mucous membrane 714974000
Eye / vision finding 118235002
Head finding 406122000
Skin finding 106076001
Developmental disorder 5294002
Disorder of skin and/or subcutaneous tissue 80659006
Congenital disease 66091009
Skin or mucosa lesion 247440002
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

Eye / vision finding 118235002

Visual system disorder 128127008

Congenital anomaly of visual system 127329003

Congenital anomaly of eye 19416009

Congenital oculocutaneous hypopigmentation 61649007

SNOMED CT code