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714254003: Abdominal organomegaly (disorder)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3299607019 Abdominal organomegaly en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3299636019 Abdominal organomegaly (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core


35 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Abdominal organomegaly Is a Disorder of abdomen (disorder) true Inferred relationship Some
Abdominal organomegaly Associated morphology Enlargement (morphologic abnormality) true Inferred relationship Some 1
Abdominal organomegaly Finding site Abdominalorgan false Inferred relationship Some 1
Abdominal organomegaly Finding site abdominalt organ som helhed false Inferred relationship Some 1
Abdominal organomegaly Is a Abdominal organ finding true Inferred relationship Some
Abdominal organomegaly Finding site Entire organ within abdominopelvic cavity true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group
Splenomegaly Is a True Abdominal organomegaly Inferred relationship Some
Large ovary Is a True Abdominal organomegaly Inferred relationship Some
Megaloappendix Is a True Abdominal organomegaly Inferred relationship Some
Large liver Is a True Abdominal organomegaly Inferred relationship Some
Congenital megalogastria Is a True Abdominal organomegaly Inferred relationship Some
Enlarged adrenal gland Is a True Abdominal organomegaly Inferred relationship Some
A rare genetic primary immunodeficiency disorder with characteristics of severe congenital neutropenia, bone marrow fibrosis and neutrophil dysfunction which is refractory to granulocyte colony-stimulating factor, manifesting with life-threatening infections and/or deep-seated abscesses, hepato/splenomegaly, thrombocytopenia, hypergammaglobulinemia, anemia with reticulocytosis and nephromegaly. Other reported features include osteosclerosis and neurological abnormalities (for example developmental delay, cortical blindness, hearing loss, thin corpus callosum or dysrhythmia on EEG). Caused by homozygous mutation in the VPS45 gene on chromosome 1q. Is a True Abdominal organomegaly Inferred relationship Some

This concept is not in any reference sets

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