Human Phenotype Ontology 
Grandparent Node:
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Abnormal spleen morphology (HP:0025408)help
Grandparent Node:
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Visceromegaly (HP:0003271)help
Parent Node:
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Splenomegaly (HP:0001744)help
..Starting node
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Fluctuating splenomegaly (HP:0006268)help
Term ID: 6268
Name: Fluctuating splenomegaly
Synonym:
Definition: Intermittently increased size of the spleen.
Comments:
Reference: HP:0006268
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0006268HP:0006268Fluctuating splenomegaly0MVK CL E G H45987530OMIM:610377Mevalonic aciduria.150
HP:0006268HP:0006268Fluctuating splenomegaly0TPP2 CL E G H717412016OMIM:619220IMMUNODEFICIENCY 78 WITH AUTOIMMUNITY AND DEVELOPMENTAL DELAY; IMD78


Genes (2) :MVK TPP2

Diseases (2) :OMIM:610377 OMIM:619220
 

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