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BabyScreen+ newborn screening v0.1377 RSPH4A Zornitza Stark Marked gene: RSPH4A as ready
BabyScreen+ newborn screening v0.1377 RSPH4A Zornitza Stark Gene: rsph4a has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.1377 RSPH4A Zornitza Stark Phenotypes for gene: RSPH4A were changed from Ciliary dyskinesia, primary to Ciliary dyskinesia, primary, 11 (MIM#612649)
BabyScreen+ newborn screening v0.1376 RSPH4A Zornitza Stark Classified gene: RSPH4A as Red List (low evidence)
BabyScreen+ newborn screening v0.1376 RSPH4A Zornitza Stark Gene: rsph4a has been classified as Red List (Low Evidence).
BabyScreen+ newborn screening v0.1375 RSPH4A Zornitza Stark reviewed gene: RSPH4A: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Ciliary dyskinesia, primary, 11 (MIM#612649); Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
BabyScreen+ newborn screening v0.0 RSPH4A Zornitza Stark gene: RSPH4A was added
gene: RSPH4A was added to gNBS. Sources: BabySeq Category A gene,Expert Review Green
Mode of inheritance for gene: RSPH4A was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: RSPH4A were set to Ciliary dyskinesia, primary