|
polyneuropathy, organomegaly, endocrinopathy, m protein, and skin changes syndrome
|
D016878 |
|
|
autosomal dominant endosteal hyperostosis
|
11878 |
|
|
ichthyosis oligophrenia epilepsy syndrome
|
C535878 |
|
|
dwarfism ichthyosiform erythroderma mental deficiency syndrome
|
C535878 |
|
|
onchocerciasis of eyeball of camera-type eye
|
5878 |
|
|
autosomal dominant familial spastic paraplegia type 3
|
10878 |
|
|
obsolete nodular fasciitis
|
18785.0 |
|
|
Chapare hemorrhagic fever
|
17878 |
|
|
TERT pulmonary fibrosis and/or bone marrow failure, Telomere-related
|
13878 |
|
|
tension vascular headache
|
D018781 |
|
|
obsolete autoimmune hemolytic anemia
|
8784.0 |
|
|
anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane
|
8789 |
|
|
optic atrophy, hereditary
|
43878 |
|
|
iron-handling disorder, hereditary
|
8788 |
|
