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Non-spherocytic hemolytic anemia due to hexokinase deficiency
1 OMIM reference -
1 associated gene
38 connected diseases
No signs/symptoms info
Disease Type of connection
Charcot-Marie-Tooth disease type 4G
Young adult-onset Parkinsonism
LIG4 syndrome
Omenn syndrome
Amyotrophic lateral sclerosis
Argininosuccinic aciduria
Autosomal dominant nonsyndromic sensorineural deafness type DFNA
Burkitt lymphoma
Combined oxidative phosphorylation defect type 4
Cowden syndrome
Dedifferentiated liposarcoma
Frontotemporal dementia with motor neuron disease
Giant cell glioblastoma
Gliosarcoma
Hereditary cerebral cavernous malformation
Juvenile amyotrophic lateral sclerosis
Myxofibrosarcoma
Myxoid / round cell liposarcoma
Precursor T-cell acute lymphoblastic leukemia
Primary ciliary dyskinesia
Proteus syndrome
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency
Sandhoff disease, adult form
Sandhoff disease, infantile form
Sandhoff disease, juvenile form
Tay-Sachs disease, B variant, adult form
Tay-Sachs disease, B variant, infantile form
Tay-Sachs disease, B variant, juvenile form
Tay-Sachs disease, B1 variant
Well-differentiated liposarcoma
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
Hereditary pheochromocytoma-paraganglioma
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare hematologic disease
Classification (ICD10):
- Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -
Epidemiological data:
Class of prevalence: <1 / 1 000 000
Average age onset: -
Average age of death: -
Type of inheritance: autosomal recessive
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
HK1 P19367142600
No signs/symptoms info available.