Activity
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3 actions
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| Fetal anomalies v8.26 | CDK4 | Ida Ertmanska commented on gene: CDK4 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.25 | CDK4 | Tessa Homfray reviewed gene: CDK4: Rating: AMBER; Mode of pathogenicity: ; Publications: 40210435; Phenotypes: microcephaly 31, primary, autosomal recessive, MONDO:0980991, Short stature, HP:0004322, Microcephaly 31, primary, autosomal recessive, OMIM:621507; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Fetal anomalies v8.23 | CDK4 |
Ida Ertmanska gene: CDK4 was added gene: CDK4 was added to Fetal anomalies. Sources: Expert Review Amber,NHS GMS Mode of inheritance for gene: CDK4 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CDK4 were set to 40210435 Phenotypes for gene: CDK4 were set to microcephaly 31, primary, autosomal recessive, MONDO:0980991; Short stature, HP:0004322; Microcephaly 31, primary, autosomal recessive, OMIM:621507 |
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