Human Phenotype Ontology 
Grandparent Node:
expandAbnormal cellular phenotype (HP:0025354)help
Parent Node:
expandAbnormal cell morphology (HP:0025461)help
..Starting node
..expandAbnormal lysosomal morphology (HP:0031340)help
Term ID: 31340
Name: Abnormal lysosomal morphology
Synonym:
Definition: A structural anomaly of lysosomes, membrane-enclosed organelles that contain an array of enzymes capable of catabolizing proteins, nucleic acids, carbohydrates, and lipids.
Comments:
Reference: HP:0031340
Genes and Diseases:
 
       Child Nodes:
........expandZebra bodies (HP:0031361) help

 Sister Nodes: 
..expandAbnormal buccal mucosa cell morphology (HP:0031476) help
..expandAbnormal cardiomyocyte morphology (HP:0031331) help
..expandAbnormal chromosome morphology (HP:0031411) help
..expandAbnormal Langerhans cell morphology (HP:0031871) 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:0031340HP:0031340Abnormal lysosomal morphology0 CL E G H
HP:0031340HP:0031361Zebra bodies1 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.