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Condition

Griscelli syndrome type 3

Congenital Malformations and Chromosomal Abnormalities

Griscelli syndrome type 3 is a disorder of melanosome transport that presents initially with hypopigmentation.

Facts
Classification
ICD-10 Chapter
XVII: Congenital Malformations, Deformations and Chromosomal Abnormalities 1
Communicable or Non-communicable
Non-Communicable 2
Transmission Route
Non-Transmissible 2
Causative Agent
Causative Agent (category)
Genetic / Hereditary 3
Sources
1. Wikipedia: ICD-10
WikipediaList of chapters, Chapter XVII
Quote, List of chapters, Chapter XVII
Congenital malformations, deformations and chromosomal abnormalities
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2. Wikipedia: Non-communicable disease
Wikipedia
  • Lead section, transmission-route statement (inferred from disease-category)
    Genetic disorders are caused by errors in genetic information that produce diseases in the affected people.
  • Inherited/genetic diseases section
    Genetic disorders are caused by errors in genetic information that produce diseases in the affected people.
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3. Orphanet (INSERM): Orphanet: Griscelli syndrome type 3 (ORPHA:79478)
Orphanet (INSERM)DisorderGeneAssociation
Quote, DisorderGeneAssociation
"DisorderGeneAssociationType": "Disease-causing germline mutation(s) in"
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