^ http://www.ebi.ac.uk/efo/EFO_0007157

Aspergillosis is an infection, growth, or allergic response caused by the Aspergillus fungus. There are several different kinds of aspergillosis. One kind is allergic bronchopulmonary aspergillosis (also called ABPA), a condition where the fungus causes allergic respiratory symptoms similar to asthma, such as wheezing and coughing, but does not actually invade and destroy tissue. Another kind of aspergillosis is invasive aspergillosis. This infection usually affects people with weakened immune systems due to cancer, AIDS, leukemia, organ transplantation, chemotherapy, or other conditions or events that reduce the number of normal white blood cells. In this condition, the fungus invades and damages tissues in the body. Invasive aspergillosis most commonly affects the lungs, but can also cause infection in many other organs and can spread throughout the body (commonly affecting the kidneys and brain). Aspergilloma , a growth (fungus ball) that develops in an area of previous lung disease such as tuberculosis or lung abscess , is a third kind of aspergillosis. This type of aspergillosis is composed of a tangled mass of fungus fibers, blood clots, and white blood cells. The fungus ball gradually enlarges, destroying lung tissue in the process, but usually does not spread to other areas. [ https://rarediseases.info.nih.gov/diseases/5856/aspergillosis ]

An opportunistic mycosis that involves a spectrum of diseases of humans and animals caused by members of the genus Aspergillus infecting lungs, brain, kidney,heart, bone, eyes, sinuses, skin and gastrointestinal tract. It is a serious illnesses in people with a weakened immune system. [ http://www.ebi.ac.uk/ontology/webulous#OPPL_pattern ]

Synonyms: Aspergillosis, aspergillosis, infection due to Aspergillus, Infection due to Aspergillus

Term info

database cross reference
  • DOID:13564 (http://www.ebi.ac.uk/ontology/webulous#OPPL_pattern)
  • MONDO:0005657
  • ICD10:B44 (MONDO:equivalentTo)
  • CSP:1988-4002 (DOID:13564)
  • ICD10:B44.2 (Orphanet:1163)
  • DOID:13564 (MONDO:equivalentTo)
  • GARD:0005856 (MONDO:equivalentTo)
  • ICD10:B44.7 (Orphanet:1163)
  • UMLS:C0004030 (Orphanet:1163)
  • MESH:D001228 (Orphanet:1163)
  • MedDRA:10003488 (Orphanet:1163)
  • ICD10:B44.8 (Orphanet:1163)
  • ICD9:117.3 (i2s)
  • SCTID:65553006 (MONDO:kboom-pr-1.00/0.80/9.44)
  • NCIT:C2886 (MONDO:kboom-pr-1.00/0.87/15.87)
  • COHD:434281 (MONDO:equivalentTo)
  • ICD10:B44.0 (Orphanet:1163)
  • ICD10:B44.9 (Orphanet:1163)
  • MSH:D001228 (http://www.ebi.ac.uk/ontology/webulous#OPPL_pattern)
  • ICD10:B44.1 (Orphanet:1163)
  • Orphanet:1163 (MONDO:equivalentTo)

gard_rare, ordo_disease


http://identifiers.org/snomedct/187492008, http://identifiers.org/snomedct/154408001, http://identifiers.org/snomedct/266218008, http://identifiers.org/snomedct/187087004


http://purl.obolibrary.org/obo/NCIT_C2886, http://linkedlifedata.com/resource/umls/id/C0004030, http://purl.obolibrary.org/obo/DOID_13564, http://identifiers.org/meddra/10003488, http://identifiers.org/mesh/D001228, http://purl.obolibrary.org/obo/Orphanet_1163, http://identifiers.org/snomedct/65553006



see also


term editor

Sirarat Sarntivijai