KCTD2
Description
The KCTD2 (potassium channel tetramerization domain containing 2) is a protein-coding gene located on chromosome 17.
KCTD2 is also known as -.
Associated Diseases
- Alzheimer disease
- macrothrombocytopenia, isolated, 2, autosomal dominant
- thrombocytopenia 4
- autosomal dominant macrothrombocytopenia
- beta-thalassemia-X-linked thrombocytopenia syndrome
- platelet-type bleeding disorder 9
- platelet-type von Willebrand disease
- thrombocythemia 2
- thrombocytopenia 7
- familial isolated congenital asplenia
- platelet-type bleeding disorder 15
- X-linked sideroblastic anemia 1
- monosomy 7 myelodysplasia and leukemia syndrome 1
- platelet-type bleeding disorder 10
- thrombocytopenia 2
- von Voss-Cherstvoy syndrome
- autosomal dominant nonsyndromic hearing loss 1
- bleeding disorder, platelet-type, 24
