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Follicular lymphoma
1 OMIM reference -
4 associated genes
115 connected diseases
14 signs/symptoms
Disease Type of connection
Intravascular large B-cell lymphoma
Precursor B-cell acute lymphoblastic leukemia
Bullous pemphigoid
Diffuse cutaneous systemic sclerosis
Limited cutaneous systemic sclerosis
Limited systemic sclerosis
MALT lymphoma
Mantle cell lymphoma
Narcolepsy without cataplexy
Narcolepsy-cataplexy
Primary mediastinal large B-cell lymphoma
Sarcoidosis
Amyotrophic lateral sclerosis
Noonan syndrome
Familial pancreatic carcinoma
Familial isolated dilated cardiomyopathy
Pilocytic astrocytoma
Acute promyelocytic leukemia
MODY syndrome
LEOPARD syndrome
Essential thrombocythemia
Behavioral variant of frontotemporal dementia
Progressive non-fluent aphasia
Semantic dementia
Familial prostate cancer
Zonular cataract
Distal 22q11.2 microdeletion syndrome
Costello syndrome
Juvenile myelomonocytic leukemia
Linear nevus sebaceus syndrome
Precursor T-cell acute lymphoblastic leukemia
Coffin-Siris syndrome
Pseudohypoaldosteronism type 2E
Microphthalmia, Lenz type
Oculofaciocardiodental syndrome
2q37 microdeletion syndrome
Graham Little-Piccardi-Lassueur syndrome
Adrenocortical carcinoma
Autoimmune lymphoproliferative syndrome with recurrent infections
B-cell chronic lymphocytic leukemia
Giant cell glioblastoma
Gliosarcoma
Li-Fraumeni syndrome
Papilloma of choroid plexus
Peters anomaly
Hereditary persistence of fetal hemoglobin - beta-thalassemia
CADDS
Proximal spinal muscular atrophy type 1
Proximal spinal muscular atrophy type 2
Proximal spinal muscular atrophy type 3
Proximal spinal muscular atrophy type 4
Severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome
Early-onset autosomal dominant Alzheimer disease
Muscular dystrophy, Selcen type
Corneal intraepithelial dyskeratosis with palmoplantar hyperkeratosis and laryngeal dyskeratosis
Vitiligo-associated autoimmune disease
Burkitt lymphoma
Cardiofaciocutaneous syndrome
Hereditary nonpolyposis colon cancer
Hereditary breast and ovarian cancer syndrome
Hereditary breast cancer
Hereditary site-specific ovarian cancer syndrome
Primary peritoneal carcinoma
Familial dementia, British type
Familial dementia, Danish type
Pseudohypoaldosteronism type 2B
Spinocerebellar ataxia type 15 / 16
Spinocerebellar ataxia type 29
Alternating hemiplegia of childhood
Autosomal recessive nonsyndromic intellectual deficit
Benign paroxysmal torticollis of infancy
COFS syndrome
Cranioectodermal dysplasia
Familial or sporadic hemiplegic migraine
Familial paroxysmal ataxia
Hereditary sensory and autonomic neuropathy type 1
Hyperinsulinism due to HNF1A deficiency
Hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies
Kleefstra syndrome due to 9q34 microdeletion
Kleefstra syndrome due to a point mutation
Short rib-polydactyly syndrome, Verma-Naumoff type
Spinocerebellar ataxia type 6
Wolcott-Rallison syndrome
Xeroderma pigmentosum complementation group G
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
Young adult-onset Parkinsonism
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Carnitine palmitoyl transferase 1A deficiency
17p13.3 microduplication syndrome
Adult-onset distal myopathy due to VCP mutation
Alpha-crystallinopathy
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Common variable immunodeficiency
Distal 17p13.3 microdeletion syndrome
Familial rhabdoid tumor
Fatal infantile hypertonic myofibrillar myopathy
Fleck corneal dystrophy
Hypohidrotic ectodermal dysplasia with immunodeficiency
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Incontinentia pigmenti
Miller-Dieker syndrome
Posterior polar cataract
Spastic paraplegia - Paget disease of bone
Wolfram syndrome
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Autosomal thrombocytopenia with normal platelets
Myelofibrosis with myeloid metaplasia
Acrokeratosis verruciformis of Hopf
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Autoimmune lymphoproliferative syndrome
Darier disease
Large congenital melanocytic nevus
Phakomatosis pigmentokeratotica
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
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:
1 OMIM reference -
1 MeSH reference: D008224
Gene symbol UniProt reference OMIM reference
BCL2 P10415151430
BCL6 P41182109565
HLA-DRB1 P04229142857
IGH Q6P089
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