|
x-linked 5 spinocerebellar ataxia
|
C567478 |
|
|
Kenny-Caffey syndrome, autosomal dominant
|
7478 |
|
|
familial, X-linked mitral valve prolapse
|
C537478 |
|
|
autosomal dominant Kenny-Caffey syndrome
|
7478 |
|
|
familial mitral regurgitation
|
C537478 |
|
|
Kenny-Caffey syndrome type 2
|
7478 |
|
|
dwarfism, cortical thickening of tubular bones and transient hypocalcemia
|
7478 |
|
|
dwarfism, cortical thickening of tubular bones, and transient hypocalcemia
|
7478 |
|
|
Kenny-Caffey syndrome, type 2
|
7478 |
|
|
Kenny-Caffey syndrome, type 2; KCS2
|
http://purl.obolibrary.org/obo/MONDO_0007478 |
|
|
familial myxomatous valvular disease
|
C537478 |
|
|
spinocerebellar ataxia, x-linked 5
|
C567478 |
|
|
amelia of upper limb, unilateral
|
17478 |
|
