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723829000: Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3426308013 Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3426309017 Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4361393019 Trimorphic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5403172019 A rare disease, manifesting with idiopathic pulmonary fibrosis, hepatic nodular regenerative hyperplasia leading to portal hypertension and thrombocytopenia due to bone marrow hypoplasia. The condition was associated with 100% mortality. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3426308013 Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3426309017 Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4361393019 Trimorphic syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3426307015 Pulmonary fibrosis - hepatic hyperplasia - bone marrow hypoplasia, also named “trimorphic syndrome” (i.e. three inherited morbidities, pulmonary, hepatic and cytopenia), is a rare disease reported in 4 cases to date, manifesting with idiopathic pulmonary fibrosis, hepatic nodular regenerative hyperplasia leading to portal hypertension and thrombocytopenia due to bone marrow hypoplasia. The condition is associated with 100% mortality. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4361392012 A rare disease with three inherited morbidities; idiopathic pulmonary fibrosis, hepatic nodular regenerative hyperplasia leading to portal hypertension and thrombocytopenia due to bone marrow hypoplasia. The condition is associated with 100% mortality. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5403172019 A rare disease, manifesting with idiopathic pulmonary fibrosis, hepatic nodular regenerative hyperplasia leading to portal hypertension and thrombocytopenia due to bone marrow hypoplasia. The condition was associated with 100% mortality. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3416971001000119 Lungenfibrose - Leberhyperplasie - Knochenmarkhypoplasie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
929771000172113 syndrome de fibrose pulmonaire-hyperplasie hépatique-hypoplasie de la moelle osseuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
929771000172113 syndrome de fibrose pulmonaire-hyperplasie hépatique-hypoplasie de la moelle osseuse fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3416971001000119 Lungenfibrose - Leberhyperplasie - Knochenmarkhypoplasie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Is a Fibrosis of lung true Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Is a Bone marrow disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Is a Nodular regenerative hyperplasia of liver (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Associated morphology Nodular regenerative hyperplasia true Inferred relationship Existential restriction modifier (core metadata concept) 3
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Finding site Liver structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Associated morphology Hypoplasia true Inferred relationship Existential restriction modifier (core metadata concept) 4
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Finding site Bone marrow structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Associated morphology Fibrosis (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 5
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Finding site Lung structure true Inferred relationship Existential restriction modifier (core metadata concept) 5
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Is a Connective tissue hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Is a Idiopathic pulmonary fibrosis false Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Is a pathologie hépatique chronique true Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Clinical course Chronic (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Associated morphology Inflammation and consolidation (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Finding site Structure of interstitial tissue of lung true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Is a Lung consolidation true Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Is a Inflammatory disorder of lower respiratory tract true Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Is a Interstitial lung disease true Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Is a Inflammation of specific body organs true Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Is a Chronic lung disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome Is a Idiopathic disease true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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