Human Phenotype Ontology 
Grandparent Node:
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Abnormality of blood and blood-forming tissues (HP:0001871)help
Parent Node:
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Abnormality of bone marrow cell morphology (HP:0005561)help
..Starting node
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Abnormality of bone marrow stromal cells (HP:0012129)help
Term ID: 12129
Name: Abnormality of bone marrow stromal cells
Synonym:
Definition:
Comments:
Reference: HP:0012129
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal granulocytopoietic cell morphology (HP:0012135) help
..expandAbnormal megakaryocyte morphology (HP:0012143) help
..expandAbnormality of multiple cell lineages in the bone marrow (HP:0012145) help
..expandReduced bone-marrow pro-B cell count (HP:0020048) 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:0012129HP:0012129Abnormality of bone marrow stromal cells0RPS14 CL E G H620810387ORPHA:86841Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormalityHP:0040283 - Occasional


Genes (1) :RPS14

Diseases (1) :ORPHA:86841
 

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