paracoccidioidomycosis |
Disease ID | 963 |
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Disease | paracoccidioidomycosis |
Definition | A mycosis affecting the skin, mucous membranes, lymph nodes, and internal organs. It is caused by Paracoccidioides brasiliensis. It is also called paracoccidioidal granuloma. Superficial resemblance of P. brasiliensis to Blastomyces brasiliensis (BLASTOMYCES) may cause misdiagnosis. |
Synonym | [x]paracoccidioidomycosis, unspecified [x]paracoccidioidomycosis, unspecified (disorder) blastomycosis, south american brazilian blastomycosis granuloma, paracoccidioidal infection by blastomyces brasiliensis infection by paracoccidioides brasiliensis lutz-splendore-almeida disease mucocutaneous south american blastomycosis mucocutaneous-lymphangitic paracoccidioidomycosis mucocutaneous-lymphangitic paracoccidioidomycosis (disorder) paracoccidiodomycosis paracoccidioidal granuloma paracoccidioidal mycosis paracoccidioidomycoses paracoccidioidomycosis (disorder) paracoccidioidomycosis [disease/finding] paracoccidioidomycosis nos paracoccidioidomycosis nos (disorder) south american blastomycosis |
Orphanet | |
DOID | |
UMLS | C0030409 |
MeSH | |
SNOMED-CT | |
Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:6) C1565489 | renal insufficiency | 1 C0001175 | acquired immunodeficiency syndrome | 1 C0024299 | lymphoma | 1 C0007847 | cervical cancer | 1 C0302592 | cervical ca | 1 C0001623 | adrenal insufficiency | 1 |
Curated Gene | (Waiting for update.) |
Inferring Gene | Entrez_id | Symbol | Resource(Total Genes:2) |
Text Mined Gene | Entrez_id | Symbol | Score | Resource(Total Genes:59) 241 | ALOX5AP | 1.039 | DISEASES 310 | ANXA7 | 2.078 | DISEASES 383 | ARG1 | 1.654 | DISEASES 85316 | BAGE5 | 1.732 | DISEASES 721 | C4B | 2.012 | DISEASES 801 | CALM1 | 1.392 | DISEASES 388372 | CCL4L1 | 1.361 | DISEASES 9332 | CD163 | 1.224 | DISEASES 50489 | CD207 | 2.648 | DISEASES 959 | CD40LG | 2.03 | DISEASES 942 | CD86 | 1.914 | DISEASES 978 | CDA | 1.015 | DISEASES 1029 | CDKN2A | 1.209 | DISEASES 1038 | CDR1 | 1.144 | DISEASES 170482 | CLEC4C | 1.335 | DISEASES 171425 | CLYBL | 3.23 | DISEASES 5476 | CTSA | 1.678 | DISEASES 4283 | CXCL9 | 2.657 | DISEASES 6993 | DYNLT1 | 1.399 | DISEASES 1915 | EEF1A1 | 1.196 | DISEASES 2027 | ENO3 | 1.651 | DISEASES 51013 | EXOSC1 | 1.979 | DISEASES 100302740 | FAS-AS1 | 1.23 | DISEASES 50943 | FOXP3 | 2.506 | DISEASES 2625 | GATA3 | 1.544 | DISEASES 10755 | GIPC1 | 1.905 | DISEASES 2739 | GLO1 | 1.252 | DISEASES 10020 | GNE | 1.124 | DISEASES 29933 | GPR132 | 2.104 | DISEASES 81502 | HM13 | 1.937 | DISEASES 3320 | HSP90AA1 | 1.372 | DISEASES 3329 | HSPD1 | 2.499 | DISEASES 3586 | IL10 | 4.249 | DISEASES 3594 | IL12RB1 | 1.349 | DISEASES 3605 | IL17A | 1.727 | DISEASES 3652 | IPP | 1.418 | DISEASES 3745 | KCNB1 | 1.468 | DISEASES 987 | LRBA | 1.034 | DISEASES 4065 | LY75 | 1.433 | DISEASES 4153 | MBL2 | 1.736 | DISEASES 25834 | MGAT4C | 1.445 | DISEASES 10724 | MGEA5 | 1.962 | DISEASES 4615 | MYD88 | 1.953 | DISEASES 4843 | NOS2 | 1.753 | DISEASES 5900 | RALGDS | 1.228 | DISEASES 2889 | RAPGEF1 | 1.269 | DISEASES 5269 | SERPINB6 | 2.376 | DISEASES 5271 | SERPINB8 | 1.858 | DISEASES 200162 | SPAG17 | 1.755 | DISEASES 11005 | SPINK5 | 1.11 | DISEASES 8576 | STK16 | 3.164 | DISEASES 6850 | SYK | 1.216 | DISEASES 7096 | TLR1 | 1.781 | DISEASES 7099 | TLR4 | 2.781 | DISEASES 10333 | TLR6 | 1.157 | DISEASES 54106 | TLR9 | 1.026 | DISEASES 7124 | TNF | 3.991 | DISEASES 8784 | TNFRSF18 | 2.52 | DISEASES 7306 | TYRP1 | 1.98 | DISEASES |
Locus | (Waiting for update.) |
Disease ID | 963 |
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Disease | paracoccidioidomycosis |
Integrated Phenotype | (Waiting for update.) |
Text Mined Phenotype | HPO | Name | Sentences' Count(Total Phenotypes:5) HP:0000846 | Hypoadrenalism | 1 HP:0002665 | Lymphoma | 1 HP:0000083 | Renal insufficiency | 1 HP:0002664 | Neoplasia | 1 HP:0002721 | Immunodeficiency | 1 |
Disease ID | 963 |
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Disease | paracoccidioidomycosis |
Manually Symptom | UMLS | Name(Total Manually Symptoms:17) C2364133 | infection C2240374 | eosinophilia C1839611 | n syndrome C1546654 | granuloma C1373218 | immunosuppression C0796095 | c syndrome C0748159 | pulmonary involvement C0403447 | chronic kidney insufficiency C0238074 | chronic cor pulmonale C0037284 | skin lesions C0033680 | protein-losing enteropathy C0029408 | osteoarthritis C0029166 | oral manifestations C0021053 | immune dysfunction C0020639 | hypoproteinemia C0020455 | hypergammaglobulinemia C0001623 | adrenal failure |
Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:1) |
Manually Genotype(Total Text Mining Genotypes:0) |
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(Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
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(Waiting for update.) |
All Snps(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Annotation(Total Genotypes:0) | |
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(Waiting for update.) |
GWASdb Snp Trait(Total Genotypes:0) | |
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(Waiting for update.) |
Mapped by lexical matching(Total Items:0) |
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(Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
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(Waiting for update.) |
Disease ID | 963 |
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Disease | paracoccidioidomycosis |
Case | (Waiting for update.) |