Typhoid

General Information (adopted from Orphanet):

Synonyms, Signs: Enteric fever
Typhoidal salmonellosis
Typhoid fever
Paratyphoid fever
Number of Symptoms 29
OrphanetNr: 99745
OMIM Id:
ICD-10: A01.0
UMLs:
MeSH:
MedDRA:
Snomed:

Prevalence, inheritance and age of onset:

Prevalence: No data available.
Inheritance: Not applicable
[Orphanet]
Age of onset: All ages
[Orphanet]

Disease classification (adopted from Orphanet):

Parent Diseases: Rare form of salmonellosis
 -Rare infectious disease

Symptom Information: Sort by abundance 

1
 (HPO:0000421) Epistaxis Occasional [Orphanet] 85 / 7739
2
 (HPO:0002315) Headache Very frequent [Orphanet] 175 / 7739
3
 (HPO:0001347) Hyperreflexia Frequent [Orphanet] 363 / 7739
4
 (HPO:0000738) Hallucinations Very frequent [Orphanet] 60 / 7739
5
 (HPO:0100785) Insomnia Very frequent [Orphanet] 18 / 7739
6
 (HPO:0001276) Hypertonia Frequent [Orphanet] 317 / 7739
7
 (HPO:0004372) Reduced consciousness/confusion Occasional [Orphanet] 73 / 7739
8
 (HPO:0001337) Tremor Occasional [Orphanet] 200 / 7739
9
 (HPO:0002066) Gait ataxia Frequent [Orphanet] 327 / 7739
10
 (HPO:0002383) Encephalitis Occasional [Orphanet] 41 / 7739
11
 (HPO:0005059) Arthralgia/arthritis Frequent [Orphanet] 141 / 7739
12
 (HPO:0002027) Abdominal pain Very frequent [Orphanet] 184 / 7739
13
 (HPO:0002014) Diarrhea Occasional [Orphanet] 225 / 7739
14
 (HPO:0001744) Splenomegaly Frequent [Orphanet] 337 / 7739
15
 (HPO:0002592) Gastric ulcer Very frequent [Orphanet] 39 / 7739
16
 (HPO:0002019) Constipation Occasional [Orphanet] 194 / 7739
17
 (HPO:0002240) Hepatomegaly Frequent [Orphanet] 467 / 7739
18
 (HPO:0002242) Abnormality of the intestine Occasional [Orphanet] 42 / 7739
19
 (HPO:0002239) Gastrointestinal hemorrhage Occasional [Orphanet] 97 / 7739
20
 (HPO:0000988) Skin rash Frequent [Orphanet] 98 / 7739
21
 (HPO:0001695) Cardiac arrest Occasional [Orphanet] 87 / 7739
22
 (HPO:0011675) Arrhythmia Frequent [Orphanet] 226 / 7739
23
 (HPO:0004936) Venous thrombosis Occasional [Orphanet] 41 / 7739
24
 (HPO:0001945) Fever Very frequent [Orphanet] 218 / 7739
25
 (HPO:0002091) Restrictive ventilatory defect Occasional [Orphanet] 46 / 7739
26
 (HPO:0001324) Muscle weakness Very frequent [Orphanet] 859 / 7739
27
 (HPO:0003326) Myalgia Frequent [Orphanet] 143 / 7739
28
 ([DEL]MedDRA:10011224) Cough Occasional [Orphanet] 70 / 7739
29
 (MedDRA:10025421) Macule Frequent [Orphanet] 55 / 7739

Associated genes:

ClinVar (via SNiPA)

Gene symbol Variation Clinical significance Reference

Additional Information: