|
diabetes mellitus, Addison disease, myxedema
|
10012 |
|
|
diabetes mellitus, Addison's disease, myxedema
|
10012 |
|
|
SCN4A-related myopathy, autosomal recessive
|
100121 |
|
|
delta1-pyrroline-5-carboxylate synthetase deficiency
|
100126 |
|
|
autoimmune thyroid disease and/or type 1 diabetes-Addison disease syndrome
|
10012 |
|
|
myopathy with ptosis and mild dystrophic pattern
|
100121 |
|
|
autoimmune polyendocrine syndrome type 2
|
10012 |
|
|
autoimmune polyglandular syndrome type 2
|
10012 |
|
|
polyglandular deficiency syndrome type 2
|
10012 |
|
|
polyendocrine autoimmune syndrome, type 2
|
10012 |
|
|
polyglandular autoimmune syndrome, type 2
|
10012 |
|
|
autoimmune polyendocrine syndrome, type II
|
10012 |
|
|
autoimmune polyendocrine syndrome, type II; APS2
|
http://purl.obolibrary.org/obo/MONDO_0010012 |
|
|
X-linked syndromic intellectual disability caused by mutation in NAA10
|
100124 |
|
