|
familial Alzheimer's disease, type 3
|
11913 |
|
|
Alzheimer disease early onset type 3
|
11913 |
|
|
Alzheimer disease, familial, 3
|
11913 |
|
|
Alzheimer disease, familial, 3, with spastic paraparesis and apraxia
|
11913 |
|
|
Alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques
|
11913 |
|
|
Hirudinea infectious disease
|
1191 |
|
|
early-onset autosomal dominant Alzheimer disease caused by mutation in PSEN1
|
11913 |
|
|
obsolete autosomal dominant limb-girdle muscular dystrophy type 1C
|
11910.0 |
|
|
capillary infantile hemangioma
|
11191 |
|
|
focal segmental glomerulosclerosis 3, susceptibility to
|
11917.0 |
|
|
hemangioma, capillary infantile
|
11191 |
|
|
autosomal recessive nonsyndromic deafness 37
|
11912 |
|
|
autosomal recessive nonsyndromic deafness caused by mutation in MYO6
|
11912 |
|
|
autosomal recessive nonsyndromic deafness type 37
|
11912 |
|
