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15890002: Albinism (disorder)

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Jul 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
26917012 Albinism en Synonym Active Entire term case insensitive SNOMED CT core module
26920016 Albinismus en Synonym Active Entire term case insensitive SNOMED CT core module
742804013 Albinism (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

31 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Albinism Is a Genodermatosis false Inferred relationship Existential restriction modifier
Albinism Is a Disease of eye false Inferred relationship Existential restriction modifier
Albinism Is a Hereditary disorder of the integument false Inferred relationship Existential restriction modifier
Albinism Is a Disorder of tyrosine metabolism false Inferred relationship Existential restriction modifier
Albinism Is a Congenital anomaly of head false Inferred relationship Existential restriction modifier
Albinism Is a Congenital deficiency of pigment of skin false Inferred relationship Existential restriction modifier
Albinism Is a Disorder of skin AND/OR subcutaneous tissue of head false Inferred relationship Existential restriction modifier
Albinism Finding site Structure of eye proper false Inferred relationship Existential restriction modifier
Albinism Associated morphology Congenital deficiency false Inferred relationship Existential restriction modifier
Albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Albinism Finding site Structure of skin region false Inferred relationship Existential restriction modifier 2
Albinism Occurrence Congenital false Inferred relationship Existential restriction modifier
Albinism Finding site Skin structure false Inferred relationship Existential restriction modifier 3
Albinism Is a Disorder of eye region false Inferred relationship Existential restriction modifier
Albinism Is a Hereditary disorder of the visual system false Inferred relationship Existential restriction modifier
Albinism Finding site Eye region structure false Inferred relationship Existential restriction modifier
Albinism Is a Site-specific disorder of skin false Inferred relationship Existential restriction modifier
Albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier
Albinism Is a Congenital anomaly of eye false Inferred relationship Existential restriction modifier
Albinism Finding site Structure of eye proper false Inferred relationship Existential restriction modifier 1
Albinism Is a Disorder of pigmentation true Inferred relationship Existential restriction modifier
Albinism Is a Inborn error of metabolism true Inferred relationship Existential restriction modifier
Albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier
Albinism Is a Congenital anomaly false Inferred relationship Existential restriction modifier
Albinism Is a Congenital malformation true Inferred relationship Existential restriction modifier
Albinism Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Albinism Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 1
Albinism Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Albinism Associated morphology Decreased melanin pigmentation false Inferred relationship Existential restriction modifier 2
Albinism Associated morphology Decreased melanin pigmentation true Inferred relationship Existential restriction modifier 1
Albinism Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Albinism Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier 1
Albinism Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Waardenburg syndrome type 3 Is a False Albinism Inferred relationship Existential restriction modifier
Ocular albinism Is a True Albinism Inferred relationship Existential restriction modifier
Hypopigmentation-immunodeficiency disease Is a False Albinism Inferred relationship Existential restriction modifier
Albinoidism Is a False Albinism Inferred relationship Existential restriction modifier
Oculocutaneous albinism Is a True Albinism Inferred relationship Existential restriction modifier
Partial albinism Is a True Albinism Inferred relationship Existential restriction modifier
Woolf's syndrome Is a True Albinism Inferred relationship Existential restriction modifier
Albinism-deafness syndrome of Tietz Is a True Albinism Inferred relationship Existential restriction modifier
Ziprkowski-Margolis syndrome Is a True Albinism Inferred relationship Existential restriction modifier
Phylloid hypomelanosis Is a True Albinism Inferred relationship Existential restriction modifier
Albinism co-occurrent with hematologic disorder Is a True Albinism Inferred relationship Existential restriction modifier
Albinism with deafness syndrome Is a False Albinism Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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