|
autosomal recessive MSMD due to partial interferon gamma receptor 2 deficiency
|
17902 |
|
|
apparent mineralocorticoid EXCESS
|
9025 |
|
|
apparent mineralocorticoid EXCESS; AME
|
http://purl.obolibrary.org/obo/MONDO_0009025 |
|
|
corneal dystrophy Groenouw type II
|
9020 |
|
|
mast cell activation syndromes
|
D000090267 |
|
|
spondyloepiphyseal dysplasia, Reardon type
|
10902 |
|
|
cramps, familial adolescent
|
9027 |
|
|
corpus callosum agenesis facial anomalies Robin sequence
|
9021 |
|
|
corpus callosum agenesis neuronopathy
|
902 |
|
|
corpus callosum, agenesis of
|
9022 |
|
|
cleft Lip/palate, agenesis of clavicles and cervical vertebrae, and talipes equinovarus
|
9028 |
|
|
corpus callosum, agenesis of, with facial anomalies and ROBIN sequence
|
9021 |
|
