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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
4 associated genes
16 signs/symptoms
Childhood apraxia of speech
MALT lymphoma

FOXP2 BIRC3
FOXP1
IGH
MALT1


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
FOXP2
(0.81)
FOXP1



Citations in the biomedical literature:


Childhood apraxia of speech
FOXP2
MALT lymphoma
BIRC3 FOXP1 IGH MALT1



Childhood apraxia of speech
MALT lymphoma

Synonym(s):
- CAS
- Developmental verbal dyspraxia
- Speech and language disorder with orofacial dyspraxia
- Speech-language disorder type 1

Synonym(s):
- Extranodal marginal zone B-cell lymphoma
- MALToma
- Mucosa-associated lymphatic tissue lymphoma
- Mucosa-associated lymphoid tissue lymphoma

Classification (Orphanet):
- Rare genetic disease
- Rare neurologic disease
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Neoplasms -

Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: childhood
Average age of death: normal
Type of inheritance: autosomal dominant
Epidemiological data:
Class of prevalence: 1-9 / 100 000
Average age onset: adulthood
Average age of death: normal
Type of inheritance: multigenic/multifactorial

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

MALT lymphoma

Very frequent
- Asthenia / fatigue / weakness
- Epigastralgia / heartburn / gastric / duodenal ulcer / gastritis
- Fever / chilling
- Hematologic / blood / lymphatic cancer
- Hyperhidrosis / increased sweating
- Lung / pulmonary infiltrates
- Nausea / vomiting / regurgitation / merycism / hyperemesis
- Weight loss / loss of appetite / break in weight curve / general health alteration

Frequent
- Constipation

Occasional
- Acute abdominal pain / colic
- Chronic uveitis / blepharitis / episcleritis / scleritis / conjonctivitis / keratitis
- Defect / anomaly of lacrimal system
- Lymphadenopathy / polyadenopathies
- Mediastinal / hilar adenopathies
- Repeat respiratory infections
- Thyroid anomalies


Childhood apraxia of speech

(no data available)