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716174001: Oculocerebral hypopigmentation syndrome of Preus type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3304970016 Oculocerebral hypopigmentation syndrome of Preus type (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3304971017 Oculocerebral hypopigmentation syndrome of Preus type en Synonym Active Only initial character case insensitive SNOMED CT core module
3304972012 Oculocerebral hypopigmentation syndrome of Preus en Synonym Active Only initial character case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Oculocerebral hypopigmentation syndrome of Preus type Is a Congenital deficiency of pigment of skin true Inferred relationship Existential restriction modifier
Oculocerebral hypopigmentation syndrome of Preus type Is a Congenital anomaly of hair true Inferred relationship Existential restriction modifier
Oculocerebral hypopigmentation syndrome of Preus type Is a Autosomal recessive hereditary disorder true Inferred relationship Existential restriction modifier
Oculocerebral hypopigmentation syndrome of Preus type Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Oculocerebral hypopigmentation syndrome of Preus type Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 2
Oculocerebral hypopigmentation syndrome of Preus type Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Oculocerebral hypopigmentation syndrome of Preus type Associated morphology Congenital hypopigmentation false Inferred relationship Existential restriction modifier 3
Oculocerebral hypopigmentation syndrome of Preus type Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Oculocerebral hypopigmentation syndrome of Preus type Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Oculocerebral hypopigmentation syndrome of Preus type Finding site Hair structure false Inferred relationship Existential restriction modifier 3
Oculocerebral hypopigmentation syndrome of Preus type Is a Genetic disorder of skin pigmentation true Inferred relationship Existential restriction modifier
Oculocerebral hypopigmentation syndrome of Preus type Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Oculocerebral hypopigmentation syndrome of Preus type Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Oculocerebral hypopigmentation syndrome of Preus type Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 2
Oculocerebral hypopigmentation syndrome of Preus type Finding site Hair structure true Inferred relationship Existential restriction modifier 1
Oculocerebral hypopigmentation syndrome of Preus type Associated morphology Hypopigmentation false Inferred relationship Existential restriction modifier 2
Oculocerebral hypopigmentation syndrome of Preus type Associated morphology Hypopigmentation true Inferred relationship Existential restriction modifier 1
Oculocerebral hypopigmentation syndrome of Preus type Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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