Disease browser and phenotype portal

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

Disease Browser
Parent Node: Pigmentation Disorders (D010859)
Parent Node: Poisoning (D011041)
..Starting node ..Argyria (D001129)
Child Nodes:
Sister Nodes:
..Argyria (D001129)
..Arsenic Poisoning (D020261)
..Bites and Stings (D001733) 8
..Cadmium Poisoning (D002105)
..Carbon Tetrachloride Poisoning (D002252)
..Drug-Induced Liver Injury (D056486) 2
..Ergotism (D004881)
..Fluoride Poisoning (D005458)
..Foodborne Diseases (D005517) 7
..Gas Poisoning (D005739) 2
..Heavy Metal Toxicity (C535854)
..Lead Poisoning (D007855) 3
..Manganese Poisoning (D020149)
..Mercury Poisoning (D008630) 2
..Mycotoxicosis (D015651) 2
..Neurotoxicity Syndromes (D020258) 20
..Organophosphate Poisoning (D062025)
..Plant Poisoning (D010939) 5
..Psychoses, Substance-Induced (D011605) 1
..Water Intoxication (D014869)
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD

Term ID:	848
Name:	Argyria
Definition:	A permanent ashen-gray discoloration of the skin, conjunctiva, and internal organs resulting from long-continued use of silver salts. (Dorland, 27th ed)
Alternative IDs:
ParentIDs:	MESH:D010859\|MESH:D011041
TreeNumbers:	C17.800.621.166 \|C25.723.068
Synonyms:	Argyrias
Slim Mappings:	Skin disease
Reference:	MedGen: D001129 MeSH: D001129 OMIM: Genes:
Phenotypes
Disease Causing ClinVar Variants