01
Alport Syndrome, Mental Retardation, Midface Hypoplasia, And Elliptocytosis
alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis
- Entity Type
- Targets
- Relation Groups
- 3
- Relation Preview
- 20
Basic Information
Grouped by core information, identifiers, and descriptions.
Core Information
- Gene Symbol
- KCNE5
- Protein Name
- No data
- Gene Type
- No data
- Chromosome
- No data
- Map Location
- No data
Identifiers
- Entrez ID
- No data
- Ensembl ID
- No data
- UniProt ID
- No data
- HGNC ID
- No data
- PDB ID
- No data
Description and Extensions
- Description
- No data
Related
Related Entities
Direct relations and traceable candidates grouped by relation type.
Related Diseases
target disease8 Diseases
02
Alport Syndrome-Intellectual Disability-Midface Hypoplasia-Elliptocytosis Syndrome
alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome
03
04
Atrial Fibrillation, Familial, 1 (Disorder)
atrial fibrillation, familial, 1 (disorder)
atrial fibrillation, familial, 1 (disorder)
05
06
07
08