|
MIM:224750 - SCHOPF-SCHULZ-PASSARGE SYNDROME; SSPS
Xenbase Genes: wnt10a
Human Disease Resource: MIM
MONDO:0009145 - SchC6pf-Schulz-Passarge syndrome |
DOID:0111647 - Schopf-Schulz-Passarge syndrome |
|
MONDO:0009145 - SchC6pf-Schulz-Passarge syndrome |
DOID:0111647 - Schopf-Schulz-Passarge syndrome |