KIF23 gene related symptoms and diseases
All the information presented here about the KIF23 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: ORPHANET,HGNC,OMIM,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to KIF23 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Short stature | Very Common - Between 80% and 100% cases |
| Multiple myeloma | Very Common - Between 80% and 100% cases |
| Abnormal erythroid lineage cell morphology | Very Common - Between 80% and 100% cases |
| Abnormal proerythroblast morphology | Very Common - Between 80% and 100% cases |
| Increased total iron binding capacity | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with KIF23 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Oral cavity bleeding
- Post-partum hemorrhage
- Abnormal cellular phenotype
- Abnormal erythrocyte morphology
- Increased serum iron
- Erythroid hyperplasia
- Congenital hypoplastic anemia
- Melena
And 18 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to KIF23 gene
Here you will find a list of rare diseases related to the KIF23. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE III
Alternate names
CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE III Is also known as anemia with multinucleated erythroblasts, erythroreticulosis, hereditary benign, congenital dyserythropoietic anemia type 3, cda type 3, dyserythropoietic anemia, congenital, type iii, cda iii, cda type iii
Description
Congenital dyserythropoietic anemia type III (CDA III) is a rare form of CDA (see this term) characterized by dyserythropoiesis, with big multinucleated erythroblasts in the bone marrow, and manifesting with mild to moderate anemia.
Most common symptoms of CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE III
- Short stature
- Neoplasm
- Anemia
- Fatigue
- Headache
More info about CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE III
Search interest in KIF23
Potential gene panels for KIF23 gene
Non-immune Hydrops Panel Panel
United States.
By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center Non-immune Hydrops Panel that also includes the following genes: RIT1 RPL11 RPL35A RPL5 RPS10 RPS17 RPS19 RPS24 RPS26 SEC23B
More info about this panel United States.
Hemolytic Anemia Panel by next-generation sequencing (NGS) Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center Hemolytic Anemia Panel by next-generation sequencing (NGS) that also includes the following genes: RHAG SEC23B SLC2A1 SPTA1 SPTB TPI1 XK ATP11C ABCG5 ABCG8
More info about this panel United States.
Congenital Dyserythropoietic Anemia Panel by next-generation sequencing (NGS) Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center Congenital Dyserythropoietic Anemia Panel by next-generation sequencing (NGS) that also includes the following genes: SEC23B LPIN2 CDAN1 C15orf41 ALAS2 GATA1 KLF1 KIF23
More info about this panel United States.
KIF23 Sequencing Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center
This panel specifically test the KIF23 gene.
More info about this panel United States.
KIF23 Deletion/duplication analysis Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center
This panel specifically test the KIF23 gene.
More info about this panel United States.
Congenital Dyserythropoietic Anemia Deletion/Duplication Panel Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center Congenital Dyserythropoietic Anemia Deletion/Duplication Panel that also includes the following genes: SEC23B LPIN2 CDAN1 C15orf41 GATA1 KLF1 KIF23
More info about this panel United States.
Hemolytic Anemia Deletion/Duplication Panel Panel
United States.
By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center Hemolytic Anemia Deletion/Duplication Panel that also includes the following genes: RHAG SEC23B SLC2A1 SPTA1 SPTB TPI1 XK ABCG5 ABCG8 LPIN2
More info about this panel United States.
Erythrocytes, Anemia Panel Panel
Germany.
By CeGaT GmbH Erythrocytes, Anemia Panel that also includes the following genes: RPL11 RPL35A RPL5 RPS10 RPS17 RPS19 RPS24 RPS26 RPS7 SEC23B
More info about this panel Germany.
NGS Panel for Congenital Dyserythropoietic Anemia Panel
Spain.
By BLOODGENETICS BLOODGENETICS NGS Panel for Congenital Dyserythropoietic Anemia that also includes the following genes: SEC23B CDAN1 C15orf41 GATA1 KLF1 KIF23
More info about this panel Spain.
Hereditary Hemolytic Anemia Comprehensive Sequencing, Varies Panel
United States.
By Mayo Clinic Genetic Testing Laboratories Mayo Clinic Hereditary Hemolytic Anemia Comprehensive Sequencing, Varies that also includes the following genes: RHAG RPS19 SEC23B SLC2A1 SPTA1 SPTB TPI1 UGT1A1 XK CD59
More info about this panel United States.
KIF23 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the KIF23 gene.
More info about this panel United States.
CONGENITAL DYSERYTHROPOIETIC ANEMIA, TYPE 3 Panel
Spain.
By Laboratorio de Genetica Clinica SL
This panel specifically test the KIF23 gene.
More info about this panel Spain.
CONGENITAL DYSERYTHROPOIETIC ANEMIA, NGS PANEL Panel
Spain.
By Laboratorio de Genetica Clinica SL CONGENITAL DYSERYTHROPOIETIC ANEMIA, NGS PANEL that also includes the following genes: SEC23B CDAN1 C15orf41 GATA1 KLF1 KIF23
More info about this panel Spain.
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