raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:330021

Mercury poisoning

Synonyms: Hydrargyria · Mercurialism · Mercury intoxication

Type
Disease
Group
Disorder
Inheritance
Not applicable
Age of onset
All ages
Status
active

Mercury poisoning is caused mainly through ingestion or inhalation of any of the 3 forms of mercury, elemental, organic, and inorganic. Exposure to elemental mercury affects the pulmonary (inhalation of mercury vapors causes coughing, chills, fever, shortness of breath), dermatological (mild swelling, vesiculation, scaling, irritation, urticaria, erythema and allergic contact dermatitis accompanied by pain), and peripheral and central nervous (CNS) systems (depression, paranoia, extreme irritability, hallucinations, inability to concentrate, memory loss, hands, head, lips, tongue, jaw and eyelids tremors, weight loss, perpetually low body temperature, drowsiness, headaches, insomnia, fatigue). Exposure to inorganic mercury generally causes development of a metallic taste, local oropharyngeal pain, nausea, vomiting, bloody diarrhea, colic abdominal pain, renal dysfunction and, neurologic abnormalities; while that to organic mercury can lead to delayed neurotoxicity.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enMercury poisoningHydrargyria · Mercurialism · Mercury intoxication
frIntoxication au mercureHydrargyrie · Mercurialisme
deQuecksilbervergiftungMerkurialismus · Quecksilber-Intoxikation
esIntoxicación por mercurioEnvenenamiento por mercurio · Hidrargiria · Mercurialismo
itAvvelenamento da mercurioMercurialismo · Idrargiria · Intossicazione da mercurio
nlKwikvergiftigingHydrargyria · Kwikintoxicatie · Mercurialisme
ptEnvenenamento por mercúrioHidrargiria · Intoxicação por mercúrio · Mercurialismo
plZatrucie rtęciąIntoksykacja rtęcią · Merkurializm · Rtęcica
csOtrava rtutí= en
ukОтруєння ртуттюГідраргірія · Меркуріалізм · Ртутна інтоксикація
zh汞中毒= en
trCıva zehirlenmesiCiva zehirlenmesi · Merkürlülük · Cıva zehirlenmesi

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10T56.1Especificvalidated
ICD-11NE61NTBTindexvalidated
MONDO0018020Evalidated
MeSHD008630Evalidated
UMLSC0025427Evalidated
GARD7021Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

1 record
TypeClassValueAreaQualificationValidationSource
Point prevalence1-9 / 100 000—EuropeClass onlyValidatedEuropean Medicines Agency 2012[OTHER]

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

21 annotations · validated 2016-12-22
HPOTerm (as annotated by Orphanet)Diagnostic
Frequent (79-30%)
HP:0002500Abnormal cerebral white matter morphology
HP:0001919Acute kidney injury
HP:0002039Anorexia
HP:0001289Confusion
HP:0002094Dyspnea
HP:0001332Dystonia
HP:0002574Episodic abdominal pain
HP:0002572Episodic vomiting
HP:0003324Generalized muscle weakness
HP:0000822Hypertension
HP:0002900Hypokalemia
HP:0002615Hypotension
HP:0100785Insomnia
HP:0006515Interstitial pneumonitis
HP:0007185Loss of consciousness
HP:0002018Nausea
HP:0002098Respiratory distress
HP:0002878Respiratory failure
HP:0001250Seizure
HP:0001649Tachycardia
HP:0001337Tremor

Annotation source: 26807265[PMID]_26678598[PMID]

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Sources for this card