Sepsis

Symptom Information:

Symptom ID: HPO:0100806
Synonyms:
Septicemia (disorder) [Orphanet:54700]
Systemic infection (disorder) [Orphanet:54700]
Systemic infection [Orphanet:54700]
Septicemia [Orphanet:54700]
Sepsis severe/septicemia [Orphanet:54700]
Sepsis [Orphanet:54700]
Unspecified septicaemia [Orphanet:54700]
Sepsis [MedDRA:10040047]
Infection systemic [MedDRA:10040047]
Other specified septicaemias [MedDRA:10040047]
Other specified septicemias [MedDRA:10040047]
Pyaemia [MedDRA:10040047]
Pyemia [MedDRA:10040047]
Sepsis NOS [MedDRA:10040047]
Sepsis secondary [MedDRA:10040047]
Septicaemia [MedDRA:10040047]
Septicaemia NOS [MedDRA:10040047]
Septicemia [MedDRA:10040047]
Unspecified septicemia [MedDRA:10040047]
Septicopyemia [MedDRA:10040047]
Septicopyaemia [MedDRA:10040047]
Unspecified septicaemia [MedDRA:10040047]
Hematological infection [MedDRA:10040047]
Haematological infection [MedDRA:10040047]
Septicemia [OMIM:Septicemia]
Systemic infections [OMIM:Systemic infections]
Unspecified septicaemia [MedDRA:10060437]
Quality:
Cross references:
Orphanet:54700 "Sepsis severe/septicemia" [Orphanet:54700]
OMIM: "Septicemia" [OMIM:Septicemia]
OMIM: "Systemic infections" [OMIM:Systemic infections]
UMLS:C0243026 "Systemic infection" [Orphanet:54700]
UMLS:C0036690 "Septicemia" [Orphanet:54700]
Is a (Direct Parents):
HPO         Neonatal sepsis
HPO         Abnormality of immune system physiology
MedDRA Sepsis, bacteraemia, viraemia and fungaemia NEC
Orphanet Health status anomalies
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)
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)