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| Predominantly Antibody Deficiency v0.116 | TNFSF13 | Zornitza Stark Marked gene: TNFSF13 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predominantly Antibody Deficiency v0.116 | TNFSF13 | Zornitza Stark Gene: tnfsf13 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predominantly Antibody Deficiency v0.116 | TNFSF13 | Zornitza Stark Phenotypes for gene: TNFSF13 were changed from Hypogammaglobulinaemia to Hypogammaglobulinaemia, MONDO:0015977, TNSF13-related | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predominantly Antibody Deficiency v0.115 | TNFSF13 | Zornitza Stark Classified gene: TNFSF13 as Red List (low evidence) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predominantly Antibody Deficiency v0.115 | TNFSF13 | Zornitza Stark Gene: tnfsf13 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Predominantly Antibody Deficiency v0.110 | TNFSF13 |
Peter McNaughton gene: TNFSF13 was added gene: TNFSF13 was added to Predominantly Antibody Deficiency. Sources: Literature Mode of inheritance for gene: TNFSF13 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TNFSF13 were set to PMID: 32298700 Phenotypes for gene: TNFSF13 were set to Hypogammaglobulinaemia Review for gene: TNFSF13 was set to RED Added comment: Single patient born to consanguineous parents Sources: Literature |
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