75616009: Reticulin fibrosis (morphologic abnormality)

SNOMED CT Concept\Body structure (body structure)\Morphologically altered structure\Morphologically abnormal structure\Lesion (morphologic abnormality)\Fibrosis AND/OR repair abnormality\...

\Fibrosis\Reticulin fibrosis

\Abnormal reticulin\Increased reticulin\Reticulin fibrosis

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

125592018 Reticulin fibrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

816246019 Reticulin fibrosis (morphologic abnormality) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Reticulin fibrosis	Is a	Increased reticulin	true	Inferred relationship	Some
Reticulin fibrosis	Is a	Fibrosis	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
A rare unclassified acute myeloid leukemia characterized by an acute panmyeloid proliferation with blasts constituting more than 20% of cells in the bone marrow or peripheral blood, accompanied by fibrosis of the bone marrow. Patients typically present with acute onset of severe constitutional symptoms, bone pain, and pancytopenia. Splenomegaly is minimal or absent. The disease is rapidly progressive with poor therapy response.	Associated morphology	True	Reticulin fibrosis	Inferred relationship	Some	2
Primary myelofibrosis	Associated morphology	False	Reticulin fibrosis	Inferred relationship	Some	1
Myelofibrosis	Associated morphology	False	Reticulin fibrosis	Inferred relationship	Some	1
Primary myelofibrosis	Is a	True	Reticulin fibrosis	Inferred relationship	Some
Acute panmyelosis with myelofibrosis	Is a	False	Reticulin fibrosis	Inferred relationship	Some
A rare unclassified acute myeloid leukemia characterized by an acute panmyeloid proliferation with blasts constituting more than 20% of cells in the bone marrow or peripheral blood, accompanied by fibrosis of the bone marrow. Patients typically present with acute onset of severe constitutional symptoms, bone pain, and pancytopenia. Splenomegaly is minimal or absent. The disease is rapidly progressive with poor therapy response.	Associated morphology	False	Reticulin fibrosis	Inferred relationship	Some	3
Myelofibrosis	Associated morphology	True	Reticulin fibrosis	Inferred relationship	Some	1
Ischemic myelofibrosis	Associated morphology	True	Reticulin fibrosis	Inferred relationship	Some	1
A rare, genetic, primary immunodeficiency disorder characterized by 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 (e.g. developmental delay, cortical blindness, hearing loss, thin corpus callosum or dysrhythmia on EEG).	Associated morphology	True	Reticulin fibrosis	Inferred relationship	Some	2
Post-polycythaemia vera myelofibrosis	Associated morphology	True	Reticulin fibrosis	Inferred relationship	Some	1
Myelofibrosis due to and following essential thrombocythemia (disorder)	Associated morphology	True	Reticulin fibrosis	Inferred relationship	Some	1
Myelofibrosis caused by drug (disorder)	Associated morphology	True	Reticulin fibrosis	Inferred relationship	Some	1

This concept is not in any reference sets