Human Phenotype Ontology 
Grandparent Node:
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Neoplasm by anatomical site (HP:0011793)help
Parent Node:
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Soft tissue neoplasm (HP:0031459)help
..Starting node
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Diffuse leiomyomatosis (HP:0006756)help
Term ID: 6756
Name: Diffuse leiomyomatosis
Synonym:
Definition:
Comments:
Reference: HP:0006756
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBenign muscle neoplasm (HP:0031460) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0006756HP:0006756Diffuse leiomyomatosis0COL4A5 CL E G H1287301050Alport syndrome, X-linked recessive301050C1567742OMIM110002207303630
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (1) :COL4A5

Diseases (1) :301050
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.