Human Phenotype Ontology 
Grandparent Node:
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Recurrent infections (HP:0002719)help
Parent Node:
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Recurrent fungal infections (HP:0002841)help
..Starting node
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Recurrent Aspergillus infections (HP:0002724)help
Term ID: 2724
Name: Recurrent Aspergillus infections
Synonym: Aspergillus infections, recurrent
Definition: An increased susceptibility to Aspergillus infections, as manifested by a history of recurrent episodes of Aspergillus infections.
Comments:
Reference: HP:0002724
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandChronic mucocutaneous candidiasis (HP:0002728) help
..expandOnychomycosis (HP:0012203) help
..expandRecurrent candida infections (HP:0005401) help
..expandRecurrent interdigital mycosis (HP:0025351) help
..expandRecurrent plantar mycosis (HP:0025472) 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:0002724HP:0002724Recurrent Aspergillus infections0CEACAM3 CL E G H10841815ORPHA:586Cystic fibrosis
HP:0002724HP:0002724Recurrent Aspergillus infections0CEACAM6 CL E G H46801818ORPHA:586Cystic fibrosis1
HP:0002724HP:0002724Recurrent Aspergillus infections0CFTR CL E G H10801884ORPHA:586Cystic fibrosis1371
HP:0002724HP:0002724Recurrent Aspergillus infections0CLCA4 CL E G H228022018ORPHA:586Cystic fibrosis
HP:0002724HP:0002724Recurrent Aspergillus infections0CYBA CL E G H15352577OMIM:233690GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, CYTOCHROME b-NEGATIVE.27
HP:0002724HP:0002724Recurrent Aspergillus infections0CYBB CL E G H15362578OMIM:306400Chronic granulomatous disease, X-linked.111
HP:0002724HP:0002724Recurrent Aspergillus infections0DCTN4 CL E G H5116415518ORPHA:586Cystic fibrosis
HP:0002724HP:0002724Recurrent Aspergillus infections0EDNRA CL E G H19093179ORPHA:586Cystic fibrosis3
HP:0002724HP:0002724Recurrent Aspergillus infections0GCLC CL E G H27294311ORPHA:586Cystic fibrosis2
HP:0002724HP:0002724Recurrent Aspergillus infections0GSTM3 CL E G H29474635ORPHA:586Cystic fibrosis1
HP:0002724HP:0002724Recurrent Aspergillus infections0HFE CL E G H30774886ORPHA:586Cystic fibrosis38
HP:0002724HP:0002724Recurrent Aspergillus infections0HMOX1 CL E G H31625013ORPHA:586Cystic fibrosis3
HP:0002724HP:0002724Recurrent Aspergillus infections0KCNN4 CL E G H37836293ORPHA:586Cystic fibrosis3
HP:0002724HP:0002724Recurrent Aspergillus infections0MIF CL E G H42827097ORPHA:586Cystic fibrosis1
HP:0002724HP:0002724Recurrent Aspergillus infections0NCF1 CL E G H6533617660OMIM:233700Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type I.13
HP:0002724HP:0002724Recurrent Aspergillus infections0NCF2 CL E G H46887661OMIM:233710Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type II.67
HP:0002724HP:0002724Recurrent Aspergillus infections0SERPINA1 CL E G H52658941ORPHA:586Cystic fibrosis131
HP:0002724HP:0002724Recurrent Aspergillus infections0SLC11A1 CL E G H655610907ORPHA:586Cystic fibrosis2
HP:0002724HP:0002724Recurrent Aspergillus infections0SLC26A9 CL E G H11501914469ORPHA:586Cystic fibrosis5
HP:0002724HP:0002724Recurrent Aspergillus infections0SLC6A14 CL E G H1125411047ORPHA:586Cystic fibrosis
HP:0002724HP:0002724Recurrent Aspergillus infections0SLC9A3 CL E G H655011073ORPHA:586Cystic fibrosis7
HP:0002724HP:0002724Recurrent Aspergillus infections0STAT1 CL E G H677211362ORPHA:391487Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndromeHP:0040283 - Occasional89
HP:0002724HP:0002724Recurrent Aspergillus infections0STX1A CL E G H680411433ORPHA:586Cystic fibrosis
HP:0002724HP:0002724Recurrent Aspergillus infections0TGFB1 CL E G H704011766ORPHA:586Cystic fibrosis13
HP:0002724HP:0002724Recurrent Aspergillus infections0TOM1 CL E G H1004311982ORPHA:391487Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndromeHP:0040283 - Occasional


Genes (25) :CEACAM3 CEACAM6 CFTR CLCA4 CYBA CYBB DCTN4 EDNRA GCLC GSTM3 HFE HMOX1 KCNN4 MIF NCF1 NCF2 SERPINA1 SLC11A1 SLC26A9 SLC6A14 SLC9A3 STAT1 STX1A TGFB1 TOM1

Diseases (6) :ORPHA:586 OMIM:233690 OMIM:306400 OMIM:233700 OMIM:233710 ORPHA:391487
 

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