Activity
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| Fetal anomalies v8.26 | FAM50A | Ida Ertmanska commented on gene: FAM50A | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | FAM50A | Louise Carr reviewed gene: FAM50A: Rating: AMBER; Mode of pathogenicity: ; Publications: 32703943; Phenotypes: Armfield type of X-linked syndromic intellectual developmental disorder, OMIM:300261; Mode of inheritance: X-LINKED: hemizygous mutation in males, biallelic mutations in females | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | FAM50A |
Ida Ertmanska gene: FAM50A was added gene: FAM50A was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: FAM50A was set to X-LINKED: hemizygous mutation in males, biallelic mutations in females Publications for gene: FAM50A were set to 32703943 Phenotypes for gene: FAM50A were set to Armfield type of X-linked syndromic intellectual developmental disorder, OMIM:300261 |
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