|
deafness, neural, with atypical atopic dermatitis
|
9088 |
|
|
smith-lemli-opitz syndrome, type i
|
D019082 |
|
|
deafness, nerve type, with mesenteric diverticula of small bowel and progressive sensory neuropathy
|
9086 |
|
|
obsolete alopecia universalis
|
19081.0 |
|
|
arrhythmogenic right ventricular cardiomyopathy 13
|
908 |
|
|
arrhythmogenic right ventricular cardiomyopathy caused by mutation in CTNNA3
|
908 |
|
|
arrhythmogenic right ventricular dysplasia 13
|
908 |
|
|
arrhythmogenic right ventricular dysplasia type 13
|
908 |
|
|
arrhythmogenic right ventricular dysplasia, familial, 13
|
908 |
|
|
arrhythmogenic right ventricular dysplasia, familial, 13; ARVD13
|
http://purl.obolibrary.org/obo/MONDO_0000908 |
|
|
arrhythmogenic right ventricular dysplasia, familial, type 13
|
908 |
|
|
hyperphenylalaninemia, Bh4-deficient, type D
|
9908 |
|
|
smith-lemli-opitz syndrome, type II
|
D019082 |
|
