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109433009: Steatocystoma multiplex (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
173996010 Steatocystoma multiplex en Synonym Active Entire term case insensitive SNOMED CT core module
611931019 Steatocystoma multiplex (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1219479016 Hereditary epidermal polycystic disease en Synonym Active Entire term case insensitive SNOMED CT core module
1219480018 Sebocystomatosis en Synonym Active Entire term case insensitive SNOMED CT core module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Steatocystoma multiplex Is a Tumor-like lesion of skin false Inferred relationship Existential restriction modifier
Steatocystoma multiplex Is a Congenital anomaly of skin false Inferred relationship Existential restriction modifier
Steatocystoma multiplex Occurrence Congenital false Inferred relationship Existential restriction modifier
Steatocystoma multiplex Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Steatocystoma multiplex Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
Steatocystoma multiplex Associated morphology Sebaceous cyst false Inferred relationship Existential restriction modifier 1
Steatocystoma multiplex Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 2
Steatocystoma multiplex Is a Keratinizing cyst false Inferred relationship Existential restriction modifier
Steatocystoma multiplex Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Steatocystoma multiplex Associated morphology Cyst false Inferred relationship Existential restriction modifier 1
Steatocystoma multiplex Is a Epidermoid cyst of skin false Inferred relationship Existential restriction modifier
Steatocystoma multiplex Associated morphology Sebaceous cyst false Inferred relationship Existential restriction modifier 1
Steatocystoma multiplex Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Steatocystoma multiplex Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Steatocystoma multiplex Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Steatocystoma multiplex Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Steatocystoma multiplex Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Steatocystoma multiplex Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Steatocystoma multiplex Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Steatocystoma multiplex Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Steatocystoma multiplex Is a Congenital disease false Inferred relationship Existential restriction modifier
Steatocystoma multiplex Associated morphology Sebaceous cyst false Inferred relationship Existential restriction modifier 1
Steatocystoma multiplex Finding site Skin structure true Inferred relationship Existential restriction modifier 1
Steatocystoma multiplex Is a Sebaceous cyst of skin true Inferred relationship Existential restriction modifier
Steatocystoma multiplex Associated morphology Steatocystomas true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Steatocystoma multiplex with natal tooth syndrome Is a True Steatocystoma multiplex Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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