|
hemorrhagic nephrosonephritis
|
5784 |
|
|
hall type spondyloepimetaphyseal dysplasia with multiple dislocations
|
C535784 |
|
|
fatal infantile, due to cytochrome c oxidase deficiency cardioencephalomyopathy
|
C565784 |
|
|
Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2
|
15784 |
|
|
hantavirus hemorrhagic fever with renal syndrome
|
5784 |
|
|
hemorrhagic fever, Russian
|
http://purl.obolibrary.org/obo/MONDO_0005784 |
|
|
Puumala virus nephropathy
|
http://purl.obolibrary.org/obo/MONDO_0005784 |
|
|
cytochrome c oxidase deficiency, fatal infantile, with cardioencephalomyopathy
|
C565784 |
|
|
leptodactylic type spondyloepimetaphyseal dysplasia with multiple dislocations
|
C535784 |
|
|
fatal infantile, with cardioencephalomyopathy cytochrome c oxidase deficiency
|
C565784 |
|
|
hemorrhagic fever with renal syndrome
|
5784 |
|
|
spondyloepimetaphyseal dysplasia with multiple dislocations, hall type
|
C535784 |
|
|
spondyloepimetaphyseal dysplasia with multiple dislocations, leptodactylic type
|
C535784 |
|
