Sepsis
Symptom Information:
Symptom ID: | HPO:0100806 | |||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the immune system(HPO:0002715) Abnormality of immune system physiology(HPO:0010978) Sepsis(HPO:0100806) MedDRA: Infections and infestations(MedDRA:10021881) Infections - pathogen unspecified(MedDRA:10021879) Sepsis, bacteraemia, viraemia and fungaemia NEC(MedDRA:10040054) Sepsis(HPO:0100806) |
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Database Frequency: | 48 / 7739 | |||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alveolar echinococcosis | (Orphanet:284) |
Arthrogryposis - renal dysfunction - cholestasis | (Orphanet:2697) |
Autosomal agammaglobulinemia | (Orphanet:33110) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Barth syndrome | (Orphanet:111) |
Bullous impetigo | (Orphanet:36237) |
Chronic granulomatous disease | (Orphanet:379) |
Classic galactosemia | (Orphanet:79239) |
Combined immunodeficiency T+ B+ due to partial RAG1 deficiency | (Orphanet:231154) |
Combined immunodeficiency due to CRAC channel dysfunction | (Orphanet:169090) |
Cryptosporidiosis - chronic cholangitis - liver disease | (Orphanet:357329) |
Cyclic neutropenia | (Orphanet:2686) |
Desmoid tumor | (Orphanet:873) |
Epidermolysis bullosa simplex with pyloric atresia | (Orphanet:158684) |
Fanconi syndrome - ichthyosis - dysmorphism | (Orphanet:1981) |
Felty syndrome | (Orphanet:47612) |
Galactosemia | (Orphanet:352) |
Hereditary North American Indian childhood cirrhosis | (Orphanet:168583) |
Hirschsprung disease | (Orphanet:388) |
Hydatidosis | (Orphanet:400) |
Idiopathic pulmonary alveolar proteinosis | (Orphanet:747) |
Isolated agammaglobulinemia | (Orphanet:229717) |
Junctional epidermolysis bullosa | (Orphanet:305) |
Kostmann syndrome | (Orphanet:99749) |
Lamellar ichthyosis | (Orphanet:313) |
Legionellosis | (Orphanet:549) |
Leprechaunism | (Orphanet:508) |
Lyell syndrome | (Orphanet:537) |
Megacystis-microcolon-intestinal hypoperistalsis syndrome | (Orphanet:2241) |
Menetrier disease | (Orphanet:2494) |
Menkes disease | (Orphanet:565) |
Navajo neurohepatopathy | (Orphanet:255229) |
Neonatal diabetes mellitus | (Orphanet:224) |
Neutropenia, severe congenital, 1, autosomal dominant | (OMIM:202700) |
Omenn syndrome | (Orphanet:39041) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Purine nucleoside phosphorylase deficiency | (Orphanet:760) |
Pyomyositis | (Orphanet:764) |
Pyruvate dehydrogenase E3 deficiency | (Orphanet:2394) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Reticular dysgenesis | (Orphanet:33355) |
Severe combined immunodeficiency | (Orphanet:183660) |
Stevens-Johnson syndrome | (Orphanet:36426) |
Transient neonatal diabetes mellitus | (Orphanet:99886) |
Vitamin B12-unresponsive methylmalonic acidemia type mut0 | (Orphanet:289916) |
Wiskott-Aldrich syndrome | (Orphanet:906) |
X-linked agammaglobulinemia | (Orphanet:47) |