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Griscelli disease type 3
1 OMIM reference -
2 associated genes
3 signs/symptoms
PROTEIN INTERACTIONS: 1
Burkitt lymphoma
1 OMIM reference -
1 associated gene
No signs/symptoms info
Griscelli disease type 3
Burkitt lymphoma

MLPH
(UniProt - OMIM)
 MYC
(UniProt - OMIM)
MYO5A
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
MYO5A
(0.63)
MYC


Citations in the biomedical literature:


Griscelli disease type 3
MLPH MYO5A
Burkitt lymphoma
MYC



Griscelli disease type 3
Burkitt lymphoma

Synonym(s):
- Griscelli-Pruniéras syndrome type 3
Synonym(s):
- Small non-cleaved cell lymphoma
Classification (Orphanet):
- Rare eye disease
- Rare genetic disease
- Rare skin disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Classification (ICD10):
- Neoplasms -
Epidemiological data:
Class of prevalence: -
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
Epidemiological data:
Class of prevalence: unknown
Average age onset: variable
Average age of death: any age
Type of inheritance: sporadic
External references:
1 OMIM reference -
1 MeSH reference: C537303
External references:
1 OMIM reference -
2 MeSH references: D002051 / D008228
Griscelli disease type 3

Very frequent
- Decreased hair pigmentation / hypopigmentation of hair
- Diffuse / generalised skin hypopigmentation / cutaneous albinism

Occasional
- Iris albinism / ocular albinism


Burkitt lymphoma

(no data available)