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Myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality
1 OMIM reference -
1 associated gene
52 connected diseases
No signs/symptoms info
Disease Type of connection
Blackfan-Diamond anemia
Common variable immunodeficiency
Young adult-onset Parkinsonism
Estrogen resistance syndrome
Dedifferentiated liposarcoma
Well-differentiated liposarcoma
46,XY complete gonadal dysgenesis
46,XY partial gonadal dysgenesis
Anaplastic ependymoma
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Spinocerebellar ataxia type 12
Adrenocortical carcinoma
Amyotrophic lateral sclerosis
B-cell chronic lymphocytic leukemia
Cabezas syndrome
Chronic mucocutaneous candidiasis
Chuvash erythrocytosis
Combined immunodeficiency due to STK4 deficiency
Cornelia de Lange syndrome
Essential thrombocythemia
Familial pancreatic carcinoma
Fibronectin glomerulopathy
Frontotemporal dementia with motor neuron disease
Giant cell glioblastoma
Gliosarcoma
Glycogen storage disease due to liver phosphorylase kinase deficiency
Infantile Refsum disease
Li-Fraumeni syndrome
Mosaic variegated aneuploidy syndrome
Neonatal adrenoleukodystrophy
Papilloma of choroid plexus
Pontocerebellar hypoplasia type 1
Precursor B-cell acute lymphoblastic leukemia
Pseudohypoaldosteronism type 2E
Von Hippel-Lindau disease
Zellweger syndrome
Catecholaminergic polymorphic ventricular tachycardia
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
Acute necrotizing encephalopathy of childhood
Familial acute necrotizing encephalopathy
Familial isolated congenital asplenia
Inflammatory myofibroblastic tumor
Retinitis pigmentosa
Synonym(s):
- 5q- syndrome
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
RPS14 P62263130620
No signs/symptoms info available.