1179364009: Fetal purpura (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Purpuric disorder\Fetal purpura
\Skin AND/OR mucosa finding\Skin finding\Bleeding skin\Purpuric disorder\Fetal purpura
\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Skin lesion\Purpuric disorder\Fetal purpura

\General finding of soft tissue\Skin finding\Bleeding skin\Purpuric disorder\Fetal purpura
\General finding of soft tissue\Skin finding\Disorder of skin\Skin lesion\Purpuric disorder\Fetal purpura
\General finding of soft tissue\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Purpuric disorder\Fetal purpura
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Purpuric disorder\Fetal purpura

\Bleeding\Purpura\Purpuric disorder\Fetal purpura
\Bleeding\Bleeding skin\Purpuric disorder\Fetal purpura
\Bleeding\Fetal blood loss\Fetal purpura

\Functional finding\Disorder of hemostatic system\Purpuric disorder\Fetal purpura

\Fetal finding\Fetal disorder\Fetal blood loss\Fetal purpura

\Integumentary system finding\Disorder of integument\Disorder involving the integument of fetus OR newborn\Fetal purpura
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Purpuric disorder\Fetal purpura
\Integumentary system finding\Skin finding\Bleeding skin\Purpuric disorder\Fetal purpura
\Integumentary system finding\Skin finding\Disorder of skin\Skin lesion\Purpuric disorder\Fetal purpura

\Disease\Purpura\Purpuric disorder\Fetal purpura
\Disease\Disorder of fetus or newborn\Disorder involving the integument of fetus OR newborn\Fetal purpura
\Disease\Disorder of fetus or newborn\Fetal disorder\Fetal blood loss\Fetal purpura
\Disease\Disorder of hemostatic system\Purpuric disorder\Fetal purpura
\Disease\Disorder of body system\Skin or mucosa lesion\Lesion of skin and/or skin-associated mucous membrane\Skin lesion\Purpuric disorder\Fetal purpura
\Disease\Disorder of body system\Disorder of integument\Disorder involving the integument of fetus OR newborn\Fetal purpura
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Purpuric disorder\Fetal purpura
\Disease\Disorder of soft tissue\Soft tissue lesion\Skin lesion\Purpuric disorder\Fetal purpura
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Skin lesion\Purpuric disorder\Fetal purpura

Status: current, Sufficiently defined by necessary conditions definition status. Date: 31-Mar 2022. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

4651684017 Fetal purpura (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

4651685016 Fetal purpura en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Fetal purpura	Interprets	Hemostatic function	true	Inferred relationship	Existential restriction modifier	2
Fetal purpura	Has interpretation	Abnormal	true	Inferred relationship	Existential restriction modifier	2
Fetal purpura	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	1
Fetal purpura	Associated morphology	Purpura	true	Inferred relationship	Existential restriction modifier	1
Fetal purpura	Is a	Purpuric disorder	true	Inferred relationship	Existential restriction modifier
Fetal purpura	Is a	Disorder involving the integument of fetus OR newborn	true	Inferred relationship	Existential restriction modifier
Fetal purpura	Is a	Fetal blood loss	true	Inferred relationship	Existential restriction modifier
Fetal purpura	Occurrence	Fetal period	true	Inferred relationship	Existential restriction modifier	1

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets