Cytoscape Web
Click node...

Acute basophilic leukemia
2 associated genes
62 connected diseases
No signs/symptoms info
Disease Type of connection
Precursor T-cell acute lymphoblastic leukemia
Beta-thalassemia - X-linked thrombocytopenia
Congenital erythropoietic porphyria
Thrombocytopenia with congenital dyserythropoietic anemia
X-linked dyserythropoetic anemia with abnormal platelets and neutropenia
Coffin-Siris syndrome
Precursor B-cell acute lymphoblastic leukemia
Acute myeloid leukemia with t(8;16)(p11;p13) translocation
Acute promyelocytic leukemia
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
Rubinstein-Taybi syndrome due to CREBBP mutations
Familial multiple meningioma
Familial rhabdoid tumor
Recurrent infection due to specific granule deficiency
1p36 deletion syndrome
Shprintzen-Goldberg syndrome
Distal 22q11.2 microdeletion syndrome
Ewing sarcoma
Extraskeletal Ewing sarcoma
Isolated delta-storage pool disease
Paris-Trousseau thrombocytopenia
Peripheral primitive neuroectodermal tumor
Congenital diaphragmatic hernia
Tetralogy of Fallot
Rubinstein-Taybi syndrome due to EP300 haploinsufficiency
2q37 microdeletion syndrome
Cataract-microcornea syndrome
Cerulean cataract
Pulverulent cataract
Atypical teratoid tumor
Intellectual deficit - sparse hair - brachydactyly
Neurofibromatosis type 3
Autosomal dominant Charcot-Marie-Tooth disease type 2F
Distal hereditary motor neuropathy type 2
Inflammatory myofibroblastic tumor
Translocation renal cell carcinoma
17p11.2 microduplication syndrome
Autosomal dominant hypohidrotic ectodermal dysplasia
Chronic intestinal pseudoobstruction
Congenital short bowel syndrome
Congenital valvular dysplasia
Ehlers-Danlos syndrome with periventricular heterotopia
Familial isolated hyperparathyroidism
Familial parathyroid adenoma
Frontometaphyseal dysplasia
Hypoparathyroidism - deafness - renal disease
Intermediate maple syrup urine disease
Isolated CoQ-cytochrome C reductase deficiency
Multiple endocrine neoplasia type 1
Osteodysplasty, Melnick-Needles type
Otopalatodigital syndrome type 1
Otopalatodigital syndrome type 2
Pancytopenia due to IKZF1 mutations
Periventricular nodular heterotopia
Smith-Magenis syndrome
Terminal osseous dysplasia - pigmentary defects
Zollinger-Ellison syndrome
Primary biliary cirrhosis
Autosomal dominant hyper-IgE syndrome
Cowden syndrome
Proteus syndrome
Microphthalmia with linear skin defects syndrome
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
No OMIM references
1 MeSH reference: D015471
Gene symbol UniProt reference OMIM reference
GATA1 P15976305371
MYB P10242189990
No signs/symptoms info available.