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Idiopathic hypereosinophilic syndrome
1 OMIM reference -
3 associated genes
114 connected diseases
No signs/symptoms info
Disease Type of connection
Bilateral striopallidodentate calcinosis
Chronic myelomonocytic leukemia
Gastrointestinal stromal tumor
Precursor B-cell acute lymphoblastic leukemia
Infantile myofibromatosis
Myeloid neoplasm associated with PDGFRA rearrangement
Myeloid neoplasm associated with PDGFRB rearrangement
Unclassified chronic myeloproliferative disease
Juvenile myelomonocytic leukemia
LEOPARD syndrome
Noonan syndrome
Berardinelli-Seip congenital lipodystrophy
Cowden syndrome
Juvenile rheumatoid factor-negative polyarthritis
Oligoarticular juvenile arthritis
Dominant hypophosphatemia with nephrolithiasis or osteoporosis
Dermatofibrosarcoma protuberans
Familial multiple meningioma
Diffuse cutaneous systemic sclerosis
Heritable pulmonary arterial hypertension
Limited cutaneous systemic sclerosis
Autosomal agammaglobulinemia
SHORT syndrome
Metachondromatosis
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia
Autosomal dominant limb-girdle muscular dystrophy type 1C
Rippling muscle disease
Romano-Ward syndrome
Autosomal dominant macrothrombocytopenia
Bannayan-Riley-Ruvalcaba syndrome
Fetal and neonatal alloimmune thrombocytopenia
Glanzmann thrombasthenia
Hereditary breast and ovarian cancer syndrome
Juvenile polyposis of infancy
Lhermitte-Duclos disease
Macrocephaly-autism syndrome
Proteus syndrome
Proteus-like syndrome
Segmental outgrowth - lipomatosis - arteriovenous malformation - epidermal nevus
Squamous cell carcinoma of head and neck
Distal 22q11.2 microdeletion syndrome
Chronic mucocutaneous candidiasis
Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency
Susceptibility to viral and mycobacterial infections
Hereditary nonpolyposis colon cancer
Acute promyelocytic leukemia
Autosomal dominant hyper-IgE syndrome
Laron syndrome with immunodeficiency
Capillary malformation - arteriovenous malformation
Parkes Weber syndrome
Pilocytic astrocytoma
Giant cell glioblastoma
Gliosarcoma
46,XY partial gonadal dysgenesis
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
Peters anomaly
Amyotrophic lateral sclerosis
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation
Familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis
Familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis
Familial idiopathic steroid-resistant nephrotic syndrome with minimal changes
Giant cell arteritis
Granulomatosis with polyangiitis
Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Pediatric systemic lupus erythematosus
T-B+ severe combined immunodeficiency due to CD45 deficiency
Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
Budd-Chiari syndrome
Essential thrombocythemia
Familial thrombocytosis
Myelofibrosis with myeloid metaplasia
Polycythemia vera
17q11 microdeletion syndrome
Acute myeloblastic leukemia with maturation
Acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)
Acute myeloid leukemia with t(8;21)(q22;q22) translocation
Aleukemic mast cell leukemia
Bullous diffuse cutaneous mastocytosis
Classic mast cell leukemia
Congenital mesoblastic nephroma
Cutaneous mastocytoma
Familial thoracic aortic aneurysm and aortic dissection
Fibrosarcoma
Infantile-onset mesial temporal lobe epilepsy with severe cognitive regression
Isolated bone marrow mastocytosis
LIG4 syndrome
Loeys-Dietz syndrome type 1
Lymphoadenopathic mastocytosis with eosinophilia
Marfan syndrome type 2
Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency
Nodular urticaria pigmentosa
Omenn syndrome
Piebaldism
Plaque-form urticaria pigmentosa
Pseudoxanthomatous diffuse cutaneous mastocytosis
Smouldering systemic mastocytosis
Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
Telangiectasia macularis eruptiva perstans
Typical urticaria pigmentosa
Weaver syndrome
Megalencephaly - polymicrogyria - postaxial polydactyly - hydrocephalus
Early-onset autosomal dominant Alzheimer disease
Hereditary cerebral hemorrhage with amyloidosis, Arctic type
Hereditary cerebral hemorrhage with amyloidosis, Dutch type
Hereditary cerebral hemorrhage with amyloidosis, Flemish type
Hereditary cerebral hemorrhage with amyloidosis, Iowa type
Hereditary cerebral hemorrhage with amyloidosis, Italian type
Hereditary cerebral hemorrhage with amyloidosis, Piedmont type
Autosomal dominant nonsyndromic intellectual deficit
CLOVE syndrome
Hemimegalencephaly
Macrodactyly of fingers, unilateral
Megalencephaly-capillary malformation-polymicrogyria syndrome
Segmental progressive overgrowth syndrome with fibroadipose hyperplasia
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare hematologic disease
- Rare oncologic disease
Classification (ICD10):
- Neoplasms -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
FIP1L1 Q6UN15607686
PDGFRA P16234173490
PDGFRB P09619173410
No signs/symptoms info available.