|
heterotopia, periventricular, associated with chromosome 5q deletion
|
C567876 |
|
|
familial, 8 atrial fibrillation
|
C567802 |
|
|
spastic paraplegia-50, autosomal recessive
|
C567858 |
|
|
myopathy, myofibrillar, bag3-related
|
C567843 |
|
|
primary, 3 biliary cirrhosis
|
C567816 |
|
|
primary, 2 biliary cirrhosis
|
C567817 |
|
|
complementation group c xeroderma pigmentosum
|
C567886 |
|
|
dilated, 1BB cardiomyopathy
|
C567877 |
|
|
growth retardation, cataract, hearing loss, and unusual appearance microcephaly
|
C567849 |
|
|
diffusa, myelinosis centralis
|
D056784 |
|
|
diffusas, myelinosis centralis
|
D056784 |
|
|
developmental delay, coarse facies, and early death growth retardation
|
C567856 |
|
|
xeroderma pigmentosum, complementation group c
|
C567886 |
|
|
autosomal recessive congenital 3 cataract
|
C567835 |
|
