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1 associated gene
No signs/symptoms info
COMMON GENES: 1
1 OMIM reference -
4 associated genes
14 signs/symptoms
Limited systemic sclerosis
Follicular lymphoma

HLA-DRB1 BCL2
BCL6
HLA-DRB1
IGH


COMMON
GENES
HLA-DRB1



Citations in the biomedical literature:


Limited systemic sclerosis
HLA-DRB1
Follicular lymphoma
BCL2 BCL6 IGH



Limited systemic sclerosis
Follicular lymphoma

Synonym(s):
- Systemic sclerosis sine scleroderma

Synonym(s):
(no synonyms)

Classification (Orphanet):
- Rare cardiac disease
- Rare renal disease
- Rare respiratory disease
- Rare skin disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

Classification (ICD10):
- Diseases of the musculoskeletal system and connective tissue -
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: unknown
Average age onset: adulthood
Average age of death: -
Type of inheritance: sporadic
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: multigenic/multifactorial

External references:
No OMIM references
No MeSH references
External references:
1 OMIM reference -
1 MeSH reference: D008224

Follicular lymphoma

Very frequent
- Fever / chilling
- Hematologic / blood / lymphatic cancer
- Hyperhidrosis / increased sweating
- Lymphadenopathy / polyadenopathies
- Weight loss / loss of appetite / break in weight curve / general health alteration

Frequent
- Asthenia / fatigue / weakness
- Mediastinal / hilar adenopathies
- Splenomegaly

Occasional
- Abnormal pleura / hydrothorax / pleuresia / pleural effusion / chylothorax
- Anomalies of skin, subcutaneous tissue and mucosae
- Bone marrow / medullar infiltration
- Lymphedema
- Meningitis / meningeal syndrome
- Structural anomaly of the peritoneum


Limited systemic sclerosis

(no data available)