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Krabbe disease - Saposin A deficiency v1.2 PSAP Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIMs #611721 & #611722) and the OMIM records were last accessed on 20 December 2025.
Krabbe disease - Saposin A deficiency v1.2 PSAP Achchuthan Shanmugasundram Phenotypes for gene: PSAP were changed from to Combined SAP deficiency, OMIM:611721; Krabbe disease, atypical, OMIM:611722; PSAP-related sphingolipidosis, MONDO:0100517
Krabbe disease - Saposin A deficiency v1.1 Eleanor Williams Panel version 1.0 has been signed off on 2023-09-14
Krabbe disease - Saposin A deficiency v1.0 Eleanor Williams promoted panel to version 1.0
Krabbe disease - Saposin A deficiency v0.3 Eleanor Williams Panel types changed to GMS Rare Disease; GMS signed-off
Krabbe disease - Saposin A deficiency v0.2 Achchuthan Shanmugasundram Panel status changed from internal to public
Krabbe disease - Saposin A deficiency v0.1 PSAP Achchuthan Shanmugasundram reviewed gene: PSAP: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Krabbe disease - Saposin A deficiency v0.1 PSAP Achchuthan Shanmugasundram gene: PSAP was added
gene: PSAP was added to Krabbe disease - Saposin A deficiency. Sources: NHS GMS,Expert Review Green
Mode of inheritance for gene: PSAP was set to BIALLELIC, autosomal or pseudoautosomal
Krabbe disease - Saposin A deficiency v0.0 Achchuthan Shanmugasundram Added Panel Krabbe disease - Saposin A deficiency
Set list of related panels to R281
Set panel types to: GMS Rare Disease