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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
bone disease +     
cellulitis +     
cutaneous mycosis +     
lung disease +     
lymph node disease +     
46,XX Sex Reversal with Dysgenesis of Kidneys, Adrenals, and Lungs  
acute chest syndrome  
adiaspiromycosis 
adult respiratory distress syndrome  
allescheriosis 
alpha 1-antitrypsin deficiency  
Alpha-2-Macroglobulin Deficiency 
alveolar echinococcosis  
Bacterial Lung Diseases +   
bejel 
blastomycosis 
bone benign neoplasm +   
Bone Cysts +   
bone development disease +   
bone inflammation disease +   
Bone Malalignment +   
Bone Neoplasms +   
bone remodeling disease +   
bone resorption disease +   
bone structure disease +   
bubonic plague 
capillariasis 
Catel Manzke syndrome  
CHOPS Syndrome  
Cloverleaf Skull Micromelia Thoracic Dysplasia 
coccidioidomycosis  
Congenital Pulmonary Lymphangiectasia  
Coxa Magna 
Coxa Valga 
cutaneous liposarcoma 
Cystic Adenomatoid Malformation of Lung, Congenital 
Cystic Disease of Lung  
cystic echinococcosis  
cystic fibrosis +   
dermatomycosis +   
dermatophytosis +  
dirofilariasis 
Endocrine Bone Diseases +   
Eosinophilic Granuloma  
Expansile Bone Lesions 
Fungal Lung Diseases +   
Genu Valgum +   
Genu Varum +   
geroderma osteodysplasticum  
granular cell tumor of the sellar region 
Hamamy Syndrome  
Hemoptysis 
hepatopulmonary syndrome  
histoplasmosis +   
Ho Kaufman Mcalister Syndrome 
hyperlucent lung 
Immunoskeletal Dysplasia with Neurodevelopmental Abnormalities  
Infectious Bone Diseases +   
interstitial lung disease +   
ischemic bone disease +   
Joint Dislocations +   
Kashani Strom Utley Syndrome 
Ludwig's angina 
lung abscess 
Lung Agenesis +   
Lung Damage, Immunodeficiency and Chromosome Breakage Syndrome  
Lung Injury +   
Lung Neoplasms +   
lymph node benign neoplasm +  
lymph node cancer +  
lymph node tuberculosis +  
lymphadenitis +   
Lymphadenopathy +   
lymphangioleiomyomatosis  
maple bark strippers' lung 
Metabolic Bone Diseases +   
middle lobe syndrome  
Myoectodermal Gonadal Dysgenesis Syndrome  
NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND SKELETAL AND BRAIN ABNORMALITIES  
neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures  
newborn respiratory distress syndrome +   
obstructive lung disease +   
orbital cellulitis 
orbital disease +   
osteochondrosis +   
Osteootohepatoenteric Syndrome  
paracoccidioidomycosis +   
A primary systemic mycosis that results_in systemic fungal infection located_in mucosa, located_in lymph nodes, located_in bone, located_in skin or located_in lungs, has_material_basis_in Paracoccidioides brasiliensis. (DO)
Parasitic Lung Diseases +   
Perifolliculitis Capitis Abscedens Et Suffodiens, Familial 
phaeohyphomycosis +  
pneumonia +   
pneumonic plague 
primary hypertrophic osteoarthropathy +   
proximal symphalangism +   
pulmonary alveolar microlithiasis  
pulmonary alveolar proteinosis +   
pulmonary artery disease +   
Pulmonary Atelectasis +   
pulmonary eosinophilia +   
Pulmonary Function 
Pulmonary Hemorrhage +   
pulmonary hemosiderosis 
pulmonary hypertension +   
pulmonary immaturity 
pulmonary plasma cell granuloma  
pulmonary systemic sclerosis 
pulmonary tuberculosis +   
respiratory failure +   
scimitar syndrome +   
scleredema adultorum 
Sclerosing Bone Dysplasia, Mental Retardation 
Slipped Epiphyses +  
sparganosis 
sphenoid sinusitis +  
spinal disease +   
sporotrichosis  
syndromic microphthalmia 9  
toxocariasis +   
Tricho-Dento-Osseous Syndrome 1 
Trochlea of the Humerus, Aplasia of 
visceral leishmaniasis  
Wells Syndrome 
Whyte Murphy Syndrome 
yaws +  

Synonyms
Exact Synonyms: South American blastomycosis ;   mucocutaneous-lymphangitic paracoccidioidomycosis ;   paracoccidioidal mycosis ;   paracoccidioidomycoses
Primary IDs: MESH:D010229
Xrefs: EFO:0007417 ;   GARD:7323 ;   ICD10CM:B41 ;   ICD9CM:116.1 ;   NCI:C34891
Definition Sources: http://www.mycology.adelaide.edu.au/Mycoses/Dimorphic_systemic/Paracoccidioidomycosis/ "DO" "DO"

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