Human Phenotype Ontology 
Grandparent Node:
expand
Phenotypic abnormality (HP:0000118)help
Parent Node:
expand
obsolete Abnormal test result (HP:0500014)help
..Starting node
..expand
Abnormal flow cytometry test result (HP:0031550)help
Term ID: 31550
Name: Abnormal flow cytometry test result
Synonym:
Definition: Any abnormal result of flow cytometry, a method that suspends cells in a stream of fluid and passes them through an electronic detection apparatus in order to assess cell count or measure biomarkers or surface molecules.
Comments:
Reference: HP:0031550
Genes and Diseases:
 
       Child Nodes:
........expandReduced cell surface marker level (HP:0031551) help
................... HP:0031552 Reduced fibroblast surface marker level
................... HP:0031553 Reduced granulocyte surface marker level

 Sister Nodes: 
..expandAbnormal cardiac test (HP:0500015) 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:0031550HP:0031550Abnormal flow cytometry test result0PIGK CL E G H100268965OMIM:618879NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATROPHY, WITH OR WITHOUT SEIZURES; NEDHCAS
HP:0031550HP:0031550Abnormal flow cytometry test result0PIGM CL E G H9318318858OMIM:610293Glycosylphosphatidylinositol deficiency6
HP:0031550HP:0031551Reduced cell surface marker level1PIGK CL E G H100268965OMIM:618879NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATROPHY, WITH OR WITHOUT SEIZURES; NEDHCAS
HP:0031550HP:0031551Reduced cell surface marker level1PIGM CL E G H9318318858OMIM:610293Glycosylphosphatidylinositol deficiency6
HP:0031550HP:0031552Reduced fibroblast surface marker level2 CL E G H
HP:0031550HP:0041048Decreased expression of GPI-anchored proteins on the cell surface2PIGK CL E G H100268965OMIM:618879NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATROPHY, WITH OR WITHOUT SEIZURES; NEDHCAS
HP:0031550HP:0031553Reduced granulocyte surface marker level2PIGM CL E G H9318318858OMIM:610293Glycosylphosphatidylinositol deficiency6
HP:0031550HP:0031558Reduced fibroblast CD59 level3 CL E G H
HP:0031550HP:0031557Reduced fibroblast CD55 level3 CL E G H
HP:0031550HP:0031556Reduced granulocyte CD16 level3 CL E G H
HP:0031550HP:0031554Reduced granulocyte CD55 level3 CL E G H
HP:0031550HP:0032455Reduced granulocyte CD18 level3 CL E G H
HP:0031550HP:0031559Reduced fibroblast CD16 level3 CL E G H
HP:0031550HP:0031555Reduced granulocyte CD59 level3PIGM CL E G H9318318858OMIM:610293Glycosylphosphatidylinositol deficiency6


Genes (2) :PIGK PIGM

Diseases (2) :OMIM:618879 OMIM:610293
 

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