|
fatal infantile, with cardioencephalomyopathy cytochrome c oxidase deficiency
|
C565784 |
|
|
spondyloepimetaphyseal dysplasia with multiple dislocations, hall type
|
C535784 |
|
|
spondyloepimetaphyseal dysplasia with multiple dislocations, leptodactylic type
|
C535784 |
|
|
noonan syndrome with pigmented villonodular synovitis
|
C537846 |
|
|
hypotonia, infantile, with psychomotor retardation
|
14784 |
|
|
hypotonia, infantile, with psychomotor retardation; IHPMR
|
http://purl.obolibrary.org/obo/MONDO_0014784 |
|
|
hemorrhagic fever with renal syndrome
|
5784 |
|
|
neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements
|
32784 |
|
|
autoimmune disease with skin involvement
|
17841 |
|
|
extrinsic asthma with status asthmaticus
|
4784 |
|
|
with or without cell oxyphilia nonmedullary thyroid carcinoma
|
C537842 |
|
