Activity
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| Fetal anomalies v8.26 | TBCB | Ida Ertmanska commented on gene: TBCB | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | TBCB | Tessa Homfray reviewed gene: TBCB: Rating: AMBER; Mode of pathogenicity: ; Publications: 40856104; Phenotypes: neurodevelopmental disorder with behavioral abnormalities and childhood-onset spastic paraplegia, MONDO:0980706, Neurodevelopmental disorder with behavioral abnormalities and childhood onset spastic paraplegia, OMIM:621382; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | TBCB |
Ida Ertmanska gene: TBCB was added gene: TBCB was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: TBCB was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TBCB were set to 40856104 Phenotypes for gene: TBCB were set to neurodevelopmental disorder with behavioral abnormalities and childhood-onset spastic paraplegia, MONDO:0980706; Neurodevelopmental disorder with behavioral abnormalities and childhood onset spastic paraplegia, OMIM:621382 |
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