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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Bilineage myelodysplasia (HP:0012149)help
Term ID: 12149
Name: Bilineage myelodysplasia
Synonym:
Definition: Myelodysplasia with dysplastic changes in two of the myeloid lineages: erythroid, granulocytic, megakaryocytic.
Comments:
Reference: HP:0012149
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandMultiple lineage myelodysplasia (HP:0012148) 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:0012149HP:0012149Bilineage myelodysplasia0 CL E G H


Genes (0) :

Diseases (0) :
 

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