Cytoscape Web
Click node...

Congenital dyserythropoietic anemia type III
1 OMIM reference -
1 associated gene
17 connected diseases
No signs/symptoms info
Disease Type of connection
Hemolytic anemia due to red cell pyruvate kinase deficiency
Peutz-Jeghers syndrome
17p13.3 microduplication syndrome
Anhidrotic ectodermal dysplasia - immunodeficiency - osteopetrosis - lymphedema
Distal 17p13.3 microdeletion syndrome
Familial prostate cancer
Hypohidrotic ectodermal dysplasia with immunodeficiency
Incontinentia pigmenti
Miller-Dieker syndrome
Nuclear cataract
X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency
Childhood-onset nemaline myopathy
Congenital fiber-type disproportion myopathy
Congenital myopathy with excess of thin filaments
Intermediate nemaline myopathy
Severe congenital nemaline myopathy
Typical nemaline myopathy
Synonym(s):
- CDA III
- CDA type 3
- CDA type III
- Congenital dyserythropoietic anemia type 3
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: variable
Average age of death: normal
Type of inheritance: autosomal dominant
External references:
1 OMIM reference -
No MeSH references
Gene symbol UniProt reference OMIM reference
KIF23 Q02241605064
No signs/symptoms info available.