Human Phenotype Ontology 
Grandparent Node:
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Abnormal ocular adnexa morphology (HP:0030669)help
Parent Node:
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Abnormal nasolacrimal system morphology (HP:0000614)help
..Starting node
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Dacryocystitis (HP:0000620)help
Term ID: 620
Name: Dacryocystitis
Synonym: Dacrocystitis; Infection of the lacrimal sac
Definition: Inflammation of the nasolacrimal sac.
Comments:
Reference: HP:0000620
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal lacrimal duct morphology (HP:0011481) help
..expandAbnormal lacrimal gland morphology (HP:0011482) help
..expandAbnormal lacrimal punctum morphology (HP:0011479) help
..expandAbnormal lacrimal sac morphology (HP:3000066) 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:0000620HP:0000620Dacryocystitis0BTNL2 CL E G H562441142ORPHA:797SarcoidosisHP:0040283 - Occasional1
HP:0000620HP:0000620Dacryocystitis0FGF10 CL E G H22553666OMIM:149730Lacrimoauriculodentodigital syndrome.17
HP:0000620HP:0000620Dacryocystitis0FGFR2 CL E G H22633689OMIM:149730Lacrimoauriculodentodigital syndrome.175
HP:0000620HP:0000620Dacryocystitis0FGFR3 CL E G H22613690OMIM:149730Lacrimoauriculodentodigital syndrome.145
HP:0000620HP:0000620Dacryocystitis0HLA-DRB1 CL E G H31234948ORPHA:797SarcoidosisHP:0040283 - Occasional2
HP:0000620HP:0000620Dacryocystitis0IGSF3 CL E G H33215950OMIM:149700Lacrimal duct defectHP:0040283 - Occasional3
HP:0000620HP:0000620Dacryocystitis0LEMD3 CL E G H2359228887ORPHA:166119Isolated osteopoikilosis68
HP:0000620HP:0000620Dacryocystitis0PRMT7 CL E G H5449625557ORPHA:464288Short stature-brachydactyly-obesity-global developmental delay syndromeHP:0040283 - Occasional6
HP:0000620HP:0000620Dacryocystitis0SATB2 CL E G H2331421637ORPHA:251028SATB2-associated syndrome due to a chromosomal rearrangementHP:0040283 - Occasional34
HP:0000620HP:0000620Dacryocystitis0TP63 CL E G H862615979OMIM:604292Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3.140


Genes (10) :BTNL2 FGF10 FGFR2 FGFR3 HLA-DRB1 IGSF3 LEMD3 PRMT7 SATB2 TP63

Diseases (7) :ORPHA:797 OMIM:149730 OMIM:149700 ORPHA:166119 ORPHA:464288 ORPHA:251028 OMIM:604292
 

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