|
extremely drug-resistant tuberculoses
|
D054908 |
|
|
extensively drug-resistant tuberculosis
|
D054908 |
|
|
extremely drug-resistant tuberculosis
|
D054908 |
|
|
smith-lemli-opitz syndrome, type 2
|
D019082 |
|
|
smith-lemli-opitz syndrome, type II
|
D019082 |
|
|
obsolete alopecia universalis
|
19081.0 |
|
|
deafness, neural, with atypical atopic dermatitis
|
9088 |
|
|
deafness, conductive, with ptosis and skeletal anomalies
|
9084 |
|
|
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 |
|
