FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

63844009: Oculocutaneous albinism (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
106102018 Oculocutaneous albinism en Synonym Active Entire term case insensitive SNOMED CT core module
106104017 Complete perfect albinism en Synonym Active Entire term case insensitive SNOMED CT core module
106105016 Albinismus totalis en Synonym Active Entire term case insensitive SNOMED CT core module
106106015 Albinismus universalis en Synonym Active Entire term case insensitive SNOMED CT core module
106107012 Total albinism en Synonym Active Entire term case insensitive SNOMED CT core module
106108019 Complete universal albinism en Synonym Active Entire term case insensitive SNOMED CT core module
803172015 Oculocutaneous albinism (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1232507012 OCA - Oculocutaneous albinism en Synonym Active Entire term case sensitive SNOMED CT core module


17 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculocutaneous albinism Is a Albinism true Inferred relationship Existential restriction modifier
Oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Oculocutaneous albinism Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism Occurrence Congenital false Inferred relationship Existential restriction modifier
Oculocutaneous albinism Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
Oculocutaneous albinism Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism Is a Congenital anomaly of eye false Inferred relationship Existential restriction modifier
Oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism Is a Congenital deficiency of pigment of skin false Inferred relationship Existential restriction modifier
Oculocutaneous albinism Is a Congenital anomaly of eye false Inferred relationship Existential restriction modifier
Oculocutaneous albinism Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Oculocutaneous albinism Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Oculocutaneous albinism Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism Is a Disorder of eye proper false Inferred relationship Existential restriction modifier
Oculocutaneous albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Oculocutaneous albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 3
Oculocutaneous albinism Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism Is a Lesion of eye false Inferred relationship Existential restriction modifier
Oculocutaneous albinism Is a Anomaly of eye false Inferred relationship Existential restriction modifier
Oculocutaneous albinism Is a Genetic disorder of skin pigmentation true Inferred relationship Existential restriction modifier
Oculocutaneous albinism Is a Congenital oculocutaneous hypopigmentation true Inferred relationship Existential restriction modifier
Oculocutaneous albinism Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism Finding site Structure of eye proper true Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier 2
Oculocutaneous albinism Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier 1
Oculocutaneous albinism Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Oculocutaneous albinism Is a Autosomal recessive ocular albinism false Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group
Black locks, oculocutaneous albinism, AND deafness of the sensorineural type Is a True Oculocutaneous albinism Inferred relationship Existential restriction modifier
Tyrosinase-positive oculocutaneous albinism Is a True Oculocutaneous albinism Inferred relationship Existential restriction modifier
Tyrosinase-negative oculocutaneous albinism Is a True Oculocutaneous albinism Inferred relationship Existential restriction modifier
Autosomal dominant oculocutaneous albinism Is a False Oculocutaneous albinism Inferred relationship Existential restriction modifier
Oculocutaneous albinism type 4 Is a True Oculocutaneous albinism Inferred relationship Existential restriction modifier
Microcephalus with albinism and digital anomaly syndrome Is a True Oculocutaneous albinism Inferred relationship Existential restriction modifier
Oculocutaneous albinism type 5 Is a True Oculocutaneous albinism Inferred relationship Existential restriction modifier
Oculocutaneous albinism type 6 Is a True Oculocutaneous albinism Inferred relationship Existential restriction modifier
Oculocutaneous albinism type 7 Is a True Oculocutaneous albinism Inferred relationship Existential restriction modifier
Oculocutaneous albinism type 1 Is a True Oculocutaneous albinism Inferred relationship Existential restriction modifier
Cross syndrome Is a True Oculocutaneous albinism Inferred relationship Existential restriction modifier

This concept is not in any reference sets

Back to Start