Albinism
Autosomal recessive hereditary disorder
Congenital oculocutaneous hypopigmentation
Genetic disorder of skin pigmentation
Hereditary disorder of the visual system
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Oculocutaneous albinism (disorder)
Oculocutaneous albinism
Complete perfect albinism
OCA - Oculocutaneous albinism
Albinismus universalis
Total albinism
Albinismus totalis
Complete universal albinism
oculocutaan albinisme
OCA
Id63844009
StatusPrimitive
Associated morphologyDecreased melanin pigmentation
Finding siteSkin structure
OccurrenceCongenital
Pathological processPathological developmental process
Associated morphologyDecreased melanin pigmentation
Finding siteEye structure
OccurrenceCongenital
Pathological processPathological developmental process
DHD Diagnosis thesaurus reference set
ICD-10 complex map reference set
TargetE70.3
RuleTRUE
AdviceALWAYS E70.3
CorrelationSNOMED CT source code to target map code correlation not specified
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Black locks, oculocutaneous albinism, AND deafness of the sensorineural type
Cross syndrome
Microcephalus with albinism and digital anomaly syndrome
Oculocutaneous albinism type 1
Oculocutaneous albinism type 4
Oculocutaneous albinism type 5
Oculocutaneous albinism type 6
Oculocutaneous albinism type 7
Tyrosinase-negative oculocutaneous albinism3
Tyrosinase-positive oculocutaneous albinism4