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Acrokeratosis verruciformis of Hopf
1 OMIM reference -
1 associated gene
30 connected diseases
No signs/symptoms info
Disease Type of connection
Darier disease
Familial isolated dilated cardiomyopathy
Giant cell glioblastoma
Gliosarcoma
Burkitt lymphoma
Precursor T-cell acute lymphoblastic leukemia
Autosomal dominant hypohidrotic ectodermal dysplasia
Congenital bilateral absence of vas deferens
Cystic fibrosis
Hereditary chronic pancreatitis
Idiopathic bronchiectasis
Intermittent hydrarthrosis
Male infertility with normal virilization due to meiosis defect
TRAPS syndrome
17q11 microdeletion syndrome
Alternating hemiplegia of childhood
CLN3 disease
CLN5 disease
Combined immunodeficiency due to STK4 deficiency
Dedifferentiated liposarcoma
Estrogen resistance syndrome
Familial or sporadic hemiplegic migraine
Glycogen storage disease due to liver phosphorylase kinase deficiency
Pediatric systemic lupus erythematosus
Pseudohypoaldosteronism type 2E
Weaver syndrome
Well-differentiated liposarcoma
Young adult-onset Parkinsonism
Follicular lymphoma
Intravascular large B-cell lymphoma
Synonym(s):
(no synonyms)
Classification (Orphanet):
- Rare genetic disease
- Rare skin disease
Classification (ICD10):
- Congenital malformations, deformations and chromosomal abnormalities -
Epidemiological data:
(no data available)
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
ATP2A2 P16615108740
No signs/symptoms info available.