Human Phenotype Ontology 
Grandparent Node:
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Abnormality of the immune system (HP:0002715)help
Parent Node:
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Abnormal vascular morphology (HP:0025015)help
Parent Node:
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Abnormality of the lymphatic system (HP:0100763)help
..Starting node
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Abnormal lymphatic vessel morphology (HP:0100766)help
Term ID: 100766
Name: Abnormal lymphatic vessel morphology
Synonym: Abnormality of the lymphatic vessels
Definition: A structural anomaly of the vessel that contains or conveys lymph fluid.
Comments:
Reference: HP:0100766
Genes and Diseases:
 
       Child Nodes:
........expandHypoplasia of lymphatic vessels (HP:0003759) help
........expandLymphatic vessel neoplasm (HP:0012797) help
................... HP:0012798 Pulmonary lymphangiomyomatosis
........expandAbnormal thoracic duct morphology (HP:0031278) help
........expandLymphangiectasis (HP:0031842) help
................... HP:0002593 Intestinal lymphangiectasia
................... HP:0005183 Pericardial lymphangiectasia
................... HP:0006273 Pancreatic lymphangiectasis
................... HP:0006521 Pulmonary lymphangiectasia
................... HP:0006531 Pleural lymphangiectasia
................... HP:0008229 Thyroid lymphangiectasia
........expandAplasia of lymphatic vessels (HP:0045006) help

 Sister Nodes: 
..expandAbnormal pulmonary lymphatics (HP:0006529) help
..expandAbnormality of the lymph nodes (HP:0002733) help
..expandAbnormality of the spleen (HP:0001743) help
..expandAbnormality of the thymus (HP:0000777) help
..expandAbnormality of the tonsils (HP:0100765) help
..expandLymphangioma (HP:0100764) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0100766HP:0100766Abnormal lymphatic vessel morphology0 CL E G H
HP:0100766HP:0033986Tortuous lymphatic vessels1 CL E G H
HP:0100766HP:0031842Lymphangiectasis1 CL E G H
HP:0100766HP:0003759Hypoplasia of lymphatic vessels1 CL E G H
HP:0100766HP:0012797Lymphatic vessel neoplasm1 CL E G H
HP:0100766HP:0045006Aplasia of lymphatic vessels1 CL E G H
HP:0100766HP:0031278Abnormal thoracic duct morphology1 CL E G H
HP:0100766HP:0005183Pericardial lymphangiectasia2 CL E G H
HP:0100766HP:0006521Pulmonary lymphangiectasia2 CL E G H
HP:0100766HP:0012798Pulmonary lymphangiomyomatosis2 CL E G H
HP:0100766HP:0006531Pleural lymphangiectasia2 CL E G H
HP:0100766HP:0006273Pancreatic lymphangiectasis2 CL E G H
HP:0100766HP:0008229Thyroid lymphangiectasia2 CL E G H
HP:0100766HP:0002593Intestinal lymphangiectasia2 CL E G H


Genes (10) :ADAMTS3 CCBE1 FAT4 FLT4 HRAS MPI PIEZO1 SOX18 TSC1 TSC2

Diseases (11) :153100 218040 602579 2136 235510 616006 616843 137940 805 538 606690
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is August 2021 release.