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.

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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

SOURCES: ORPHANET OMIM


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

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

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

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

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

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

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

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

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

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

KIF23 Panel

United States.

By Fulgent Genetics Fulgent Genetics

This panel specifically test the KIF23 gene.

More info about this panel

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

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


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