FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.8.3  |  FHIR Version n/a  User: [n/a]

450937003: Acute myeloid leukemia with RBM15::MKL1 fusion (morphologic abnormality)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2012. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
2920570019 Acute myeloid leukaemia (megakaryoblastic) with t(1;22)(p13;q13); RBM15-MKL1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2921032019 Acute myeloid leukemia (megakaryoblastic) with t(1;22)(p13;q13); RBM15-MKL1 en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5143394018 Acute myeloid leukaemia with RBM15::MKL1 fusion en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5143395017 Acute myeloid leukemia with RBM15::MKL1 fusion (morphologic abnormality) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5143396016 Acute myeloid leukemia with RBM15::MKL1 fusion en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Acute myeloid leukaemia with RBM15::MKL1 fusion Is a Akut myeloid leukæmi false Inferred relationship Some
Acute myeloid leukaemia with RBM15::MKL1 fusion Is a Akut myeloid leukæmi med recidiverende genetisk abnormitet false Inferred relationship Some
Acute myeloid leukaemia with RBM15::MKL1 fusion Is a Acute myeloid leukemia (morphologic abnormality) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13) is a rare subtype of acute myeloid leukemia with recurrent cytogenetic abnormalities characterized by clonal proliferation of myeloid blasts with predominantly megakaryoblastic differentiation in the bone marrow and blood, often with extensive infiltration of the abdominal organs. It occurs typically in infants and usually presents with hepatosplenomegaly, anemia, thrombocytopenia and nonspecific symptoms related to ineffective hematopoiesis (fatigue, bleeding and bruising, recurrent infections). Myelofibrosis and fibrosis of other infiltrated organs is also characteristic of this disease. Associated morphology True Acute myeloid leukaemia with RBM15::MKL1 fusion Inferred relationship Some 1

This concept is not in any reference sets

Back to Start