Human Phenotype Ontology 
Grandparent Node:
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Blepharitis (HP:0000498)help
Parent Node:
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Posterior blepharitis (HP:0025610)help
..Starting node
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Seborrhoeic blepharitis (HP:0500046)help
Term ID: 500046
Name: Seborrhoeic blepharitis
Synonym:
Definition: Inflamation of the eyelid due to overactivity of the sebaceous gland.
Comments:
Reference: HP:0500046
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:0500046HP:0500046Seborrhoeic blepharitis0GATA1 CL E G H26234170ORPHA:79277Congenital erythropoietic porphyriaHP:0040284 - Very rare29
HP:0500046HP:0500046Seborrhoeic blepharitis0UROD CL E G H738912591ORPHA:95159Hepatoerythropoietic porphyriaHP:0040284 - Very rare31
HP:0500046HP:0500046Seborrhoeic blepharitis0UROS CL E G H739012592ORPHA:79277Congenital erythropoietic porphyriaHP:0040284 - Very rare41


Genes (3) :GATA1 UROD UROS

Diseases (2) :ORPHA:79277 ORPHA:95159
 

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