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1222705009: Familial multiple discoid fibroma (disorder)


Status: current, Primitive. Date: 31-May 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5048592016 Familial multiple trichodiscoma en Synonym Active Case insensitive SNOMED CT core
5048593014 Familial multiple discoid fibroma en Synonym Active Case insensitive SNOMED CT core
5048594015 Familial multiple discoid fibroma (disorder) en Fully specified name Active Case insensitive SNOMED CT core
5048595019 A rare genetic skin tumour disorder characterised by childhood-onset of multiple benign asymptomatic white to flesh-coloured papules predominantly located on the face, ears, neck and trunk, not associated with systemic organ involvement, associated malignancies or FLCN gene locus mutation. en Definition Active Case sensitive SNOMED CT core
5048596018 A rare genetic skin tumor disorder characterized by childhood-onset of multiple benign asymptomatic white to flesh-colored papules predominantly located on the face, ears, neck and trunk, not associated with systemic organ involvement, associated malignancies or FLCN gene locus mutation. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Familial multiple discoid fibroma Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Familial multiple discoid fibroma Is a Trichodiscoma true Inferred relationship Some
Familial multiple discoid fibroma Is a Hereditary disorder of the integument true Inferred relationship Some
Familial multiple discoid fibroma Is a Dermatosis in childhood true Inferred relationship Some
Familial multiple discoid fibroma Is a Familial neoplastic disease true Inferred relationship Some
Familial multiple discoid fibroma Occurrence Childhood true Inferred relationship Some 1
Familial multiple discoid fibroma Finding site Skin structure true Inferred relationship Some 1
Familial multiple discoid fibroma Associated morphology Follicular fibroma true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Neoplasm and/or hamartoma reference set

Problem/Diagnosis reference set

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