Myosin binding protein C1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome (disorder)
| Code | 1251451005 |
|---|---|
| Semantic tag | disorder |
| Module | international |
| Definition | primitive |
| Effective time | 20220930 |
205402004Arthrogryposis multiplex congenita
disorder
85995004Autosomal recessive hereditary disorder
disorder
29271008Camptodactyly
disorder
28204005Inherited arthrogryposis
disorder
23359005Multiple malformation syndrome with facial-limb defects as major feature
disorder
None (leaf concept).