ORPHA:730396
Invasive meningococcal disease
Synonyms: IMD
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Invasive meningococcal disease | IMD |
| fr | Infection invasive à méningocoque | IIM |
| de | Invasive Meningokokkenerkrankung | = en |
| es | Enfermedad meningocócica invasiva | EMI |
| it | Malattia meningococcica invasiva | = en |
| nl | Invasieve meningokokkenziekte | Invasieve infectie door Neisseria meningitidis · IMD · Invasieve meningokokkeninfectie |
| pt | Invasive meningococcal disease | |
| pl | Invasive meningococcal disease | = en |
| cs | Invasive meningococcal disease | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:163582Rare bacterial infectious disease
rare infectious diseases
No children.
Codes that Orphanet moved or referred to this one:
- ORPHA:33475Meningococcal meningitis moved to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
34 annotations · validated 2020-02-07| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Very frequent (99-80%) | ||
| HP:0012229 | CSF pleocytosis | |
| HP:0001945 | Fever | |
| HP:0011972 | Hypoglycorrhachia | |
| HP:0002922 | Increased CSF protein concentration | |
| HP:0031179 | Nuchal rigidity | |
| HP:0025258 | Stiff neck | |
| Frequent (79-30%) | ||
| HP:0002039 | Anorexia | |
| HP:0011227 | Elevated circulating C-reactive protein concentration | |
| HP:0002315 | Headache | |
| HP:0000967 | Petechiae | |
| HP:0000613 | Photophobia | |
| HP:0002587 | Projectile vomiting | |
| HP:0004372 | Reduced consciousness | |
| HP:0100806 | Sepsis | |
| HP:0000988 | Skin rash | |
| Occasional (29-5%) | ||
| HP:6000647 | Bulging fontanelle | |
| HP:0002329 | Drowsiness | |
| HP:0000365 | Hearing impairment | |
| HP:0002615 | Hypotension | |
| HP:0032308 | Increased circulating procalcitonin concentration | |
| HP:0002516 | Increased intracranial pressure | |
| HP:0000737 | Irritability | |
| HP:0001254 | Lethargy | |
| HP:0001085 | Papilledema | |
| HP:0003401 | Paresthesia | |
| HP:0000979 | Purpura | |
| HP:0000083 | Renal insufficiency | |
| HP:0001250 | Seizure | |
| Very rare (<4-1%) | ||
| HP:0011880 | Acute disseminated intravascular coagulation | |
| HP:0006824 | Cranial nerve paralysis | |
| HP:0002045 | Hypothermia | |
| HP:0002643 | Neonatal respiratory distress | |
| HP:0031273 | Shock | |
| HP:0001297 | Stroke | |
Run the differential on the 6 obligate / very frequent terms
Annotation source: 30860561[PMID]_31990941[PMID]_31956973[PMID]_29203096[PMID]
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/730396
- This record as JSON: /data/d/730396.json