Human Phenotype Ontology 
Grandparent Node:
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Hematological neoplasm (HP:0004377)help
Parent Node:
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Myelodysplasia (HP:0002863)help
..Starting node
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Multiple lineage myelodysplasia (HP:0012148)help
Term ID: 12148
Name: Multiple lineage myelodysplasia
Synonym:
Definition: Myelodysplasia with dysplastic changes in two or more of the myeloid lineages: erythroid, granulocytic, megakaryocytic.
Comments:
Reference: HP:0012148
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBilineage myelodysplasia (HP:0012149) help
..expandSingle lineage myelodysplasia (HP:0012150) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012148HP:0012148Multiple lineage myelodysplasia0GATA2 CL E G H26244171ORPHA:98827Unclassified myelodysplastic syndromeHP:0040282 - Frequent137
HP:0012148HP:0012148Multiple lineage myelodysplasia0RPS14 CL E G H620810387ORPHA:86841Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormalityHP:0040283 - Occasional


Genes (2) :GATA2 RPS14

Diseases (2) :ORPHA:98827 ORPHA:86841
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.