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1149090009: Multiple hamartomatous polyps (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4553724018 Multiple hamartomatous polyps en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4553725017 Multiple hamartomatous polyps (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Multiple hamartomatous polyps Is a Hamartomatous polyp true Inferred relationship Some
Multiple hamartomatous polyps Is a Multiple polyps true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Syndrome with characteristics of co-occurrence of both juvenile polyposis syndrome and hereditary hemorrhagic telangiectasia. Juvenile polyposis syndrome has characteristics of hamartomatous polyps occurring throughout the gastrointestinal tract. Hereditary hemorrhagic telangiectasia is characterized by vascular dysplasia with telangiectases of the skin, oral and nasal mucosa and arteriovenous malformation of the lungs, liver, brain and gastrointestinal tract. The syndrome is caused by heterozygous mutation in the SMAD4 gene on chromosome 18q21. Associated morphology True Multiple hamartomatous polyps Inferred relationship Some 4
Juvenile polyposis syndrome Associated morphology True Multiple hamartomatous polyps Inferred relationship Some 1
Juvenile polyposis of infancy (disorder) Associated morphology True Multiple hamartomatous polyps Inferred relationship Some 1

This concept is not in any reference sets

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