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Follicular lymphoma
1 OMIM reference -
4 associated genes
14 signs/symptoms
PROTEIN INTERACTIONS: 1
Microphthalmia, Lenz type
2 OMIM references -
2 associated genes
43 signs/symptoms
Follicular lymphoma
Microphthalmia, Lenz type

BCL2
(UniProt - OMIM)
 BCOR
(UniProt - OMIM)
BCL6
(UniProt - OMIM)
 NAA10
(UniProt - OMIM)
HLA-DRB1
(UniProt - OMIM)
IGH
(UniProt)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
BCL6
(0.9)
BCOR


Citations in the biomedical literature:


Follicular lymphoma
BCL2 BCL6 HLA-DRB1 IGH
Microphthalmia, Lenz type
BCOR NAA10



Follicular lymphoma
Microphthalmia, Lenz type

Synonym(s):
(no synonyms)

Synonym(s):
- Lenz microphthalmia
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare eye disease
- Rare genetic disease
- Rare neurologic disease
Classification (ICD10):
- Neoplasms -
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
Class of prevalence: 1-5 / 10 000
Average age onset: adulthood
Average age of death: adult
Type of inheritance: multigenic/multifactorial
Epidemiological data:
Class of prevalence: unknown
Average age onset: neonatal/infancy
Average age of death: -
Type of inheritance: x-linked recessive
External references:
1 OMIM reference -
1 MeSH reference: D008224
External references:
2 OMIM references -
No MeSH references
Follicular lymphoma
Microphthalmia, Lenz type

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


Very frequent
- Anophthalmos / anophthalmia / microphthalmos / microphthalmia
- X-linked recessive inheritance

Frequent
- Abnormal dentition / dental position / implantation / unerupted / dental ankylosis
- Agenesis / hypoplasia / aplasia of kidneys
- Camptodactyly of fingers
- Cleft lip and palate
- Clinodactyly of fifth finger
- Coloboma of iris
- Coloboma of the optic nerve
- External ear anomalies
- Glaucoma
- Hypospadias / epispadias / bent penis
- Intellectual deficit / mental / psychomotor retardation / learning disability
- Low set ears / posteriorly rotated ears
- Megaureter / hydronephrosis / pyeloureteral junction syndrome
- Microcephaly
- Microcornea
- Retinoschisis / retinal / chorioretinal coloboma
- Short stature / dwarfism / nanism
- Syndactyly of fingers / interdigital palm
- Thumb duplication / distal bifid thumb phalangeal bone
- Tooth shape anomaly
- Undescended / ectopic testes / cryptorchidia / unfixed testes
- Ureterocele / cystic dilation / dilatation of the ureter / ureterovasical stenosis

Occasional
- Auto-aggressivity / auto-mutilation
- Cataract / lens opacification
- Clavicle absent / abnormal
- Congenital cardiac anomaly / malformation / cardiopathy
- Corpus callosum / septum pellucidum total / partial agenesis
- Cryptophthalmia / ankyloblepharon / synblepharon
- Delayed dentition / eruption of teeth / lack of eruption of teeth
- Hearing loss / hypoacusia / deafness
- Kyphosis
- Long rib cage / thorax
- Lordosis
- Narrow / sloping shoulders
- Nystagmus
- Preauricular / branchial tags / appendages
- Scoliosis
- Seizures / epilepsy / absences / spasms / status epilepticus
- Speech troubles / aphasia / dysphasia / echolalia / mutism / logorrhea / dysprosodia
- Visual loss / blindness / amblyopia
- Webbed neck / pterygium colli