|
spondylometaphyseal dysplasia Algerian type
|
8478 |
|
|
spondylometaphyseal dysplasia, Algerian type
|
8478 |
|
|
AR hyperimmunoglobulin E syndrome
|
9478 |
|
|
hyper Ig E syndrome, autosomal recessive
|
9478 |
|
|
Early-onset FECD Early-onset fuchs' endothelial corneal dystrophy
|
C535478 |
|
|
autosomal dominant Kenny-Caffey syndrome
|
7478 |
|
|
congenital disorder OF glycosylation, type IIo; CDG2O
|
http://purl.obolibrary.org/obo/MONDO_0014789 |
|
|
tay-sachs disease, Pseudo-AB variant
|
C564786 |
|
|
spondylometaphyseal dysplasia Schmidt type
|
8478 |
|
|
spondylometaphyseal dysplasia, Schmidt type
|
8478 |
|
|
strictly posterior acute myocardial infarction
|
4780 |
|
|
corpus callosum, agenesis OF, with FACIAL anomalies and cerebellar ataxia
|
14787 |
|
|
corpus callosum, agenesis OF, with FACIAL anomalies and cerebellar ataxia; CCAFCA
|
http://purl.obolibrary.org/obo/MONDO_0014787 |
|
