| Panel | Mode of inheritance | Details |
|---|---|---|
2 panels | ||
R-numbers: R58 Signed-off version 5.4 | X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males) | Phenotypes McLeod syndrome with or without chronic granulomatous disease, OMIM:300842, McLeod neuroacanthocytosis syndrome, MONDO:0018945 |
Green in Rare anaemiaR-numbers: R92 Signed-off version 3.0 | X-LINKED: hemizygous mutation in males, biallelic mutations in females | Phenotypes McLeod syndrome with or without chronic granulomatous disease, OMIM:300842, McLeod neuroacanthocytosis syndrome, MONDO:0018945 |