Intestinal failure or congenital diarrhoea
Gene: CD55EnsemblGeneIds (GRCh38): ENSG00000196352
EnsemblGeneIds (GRCh37): ENSG00000196352
OMIM: 125240, Gene2Phenotype
CD55 is in 3 panels
1 review
Eleanor Williams (Genomics England Curator)
This gene has been added to the panel on the recommendation of the NHS Genomic Medicine Service and should be rated green.Created: 8 Mar 2022, 11:44 a.m. | Last Modified: 8 Mar 2022, 11:44 a.m.
Panel Version: 1.48
Details
- Mode of Inheritance
- BIALLELIC, autosomal or pseudoautosomal
- Sources
-
- Expert Review Green
- Phenotypes
-
- Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy, OMIM:226300
- OMIM
- 125240
- Clinvar variants
- Variants in CD55
- Penetrance
- None
- Panels with this gene
History Filter Activity
Created, Added New Source, Set mode of inheritance, Set Phenotypes
Ivone Leong (Genomics England Curator)gene: CD55 was added gene: CD55 was added to Intestinal failure. Sources: Expert Review Green Mode of inheritance for gene: CD55 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: CD55 were set to Complement hyperactivation, angiopathic thrombosis, and protein-losing enteropathy, OMIM:226300