|
MIM:309950 - MUSCULAR DYSTROPHY, HEMIZYGOUS LETHAL TYPE
Xenbase Genes:
Human Disease Resource: MIM
MONDO:0010676 - manual digit 2 phalanx cartilage element |
DOID:9884 - muscular dystrophy |
|
MONDO:0010676 - manual digit 2 phalanx cartilage element |
DOID:9884 - muscular dystrophy |