|
hereditary pulmonary emphysema
|
C566273 |
|
|
peritoneal scleroses, encapsulating
|
D056627 |
|
|
peritoneal sclerosis, encapsulating
|
D056627 |
|
|
alzheimer disease, familial, 1
|
C566298 |
|
|
alzheimer disease, early-onset, with cerebral amyloid angiopathy
|
C566299 |
|
|
atresia of external auditory canal and conduction deafness
|
C566245 |
|
|
hereditary benign erythroreticulosis
|
C566285 |
|
|
syndrome, peritoneal fibrosing
|
D056627 |
|
|
brachmann-de lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay
|
C566206 |
|
|
syndromes, peritoneal fibrosing
|
D056627 |
|
|
hyperlipemia with familial hypercholesterolemic xanthomatosis
|
C566263 |
|
|
alpha-1 protease inhibitor deficiency
|
C566273 |
|
