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717224002: X-linked reticulate pigmentary disorder with systemic manifestation syndrome (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
3308724010 X-linked reticulate pigmentary disorder with systemic manifestation syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3308725011 X-linked reticulate pigmentary disorder with systemic manifestation syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3308726012 Partington disease en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Is a Inherited cutaneous hyperpigmentation false Inferred relationship Existential restriction modifier
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 3
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Associated morphology Hyperpigmentation false Inferred relationship Existential restriction modifier 2
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 3
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Is a Genetic disorder of skin pigmentation true Inferred relationship Existential restriction modifier
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 1
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 1
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 1
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Associated morphology Hyperpigmentation true Inferred relationship Existential restriction modifier 1
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Is a X-linked dominant hereditary disease true Inferred relationship Existential restriction modifier
X-linked reticulate pigmentary disorder with systemic manifestation syndrome Is a Hyperpigmentation of skin 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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