|
lymphedema, hereditary, IB; LMPH1B
|
http://purl.obolibrary.org/obo/MONDO_0012765 |
|
|
radiosensitivity-immunodeficiency-dysmorphic features-learning difficulties syndrome
|
12764 |
|
|
ventricular tachycardia, catecholaminergic polymorphic, 2
|
12762 |
|
|
ventricular tachycardia, catecholaminergic polymorphic, 2; CPVT2
|
http://purl.obolibrary.org/obo/MONDO_0012762 |
|
|
ventricular tachycardia, catecholaminergic polymorphic, type 2
|
12762 |
|
|
macular degeneration, age-related, 11
|
12767 |
|
|
macular degeneration, age-related, 11; ARMD11
|
http://purl.obolibrary.org/obo/MONDO_0012767 |
|
|
macular Degeneration, age-related, type 11
|
12767 |
|
|
papilloma of buccal mucosa
|
21276 |
|
|
radiosensitivity, immunodeficiency, dysmorphic features, and learning difficulties
|
12764 |
|
|
age-related macular degeneration caused by mutation in CST3
|
12767 |
|
|
expressive language disorder
|
1276 |
|
|
prostate cancer, hereditary, 11
|
12768 |
|
|
epilepsy, idiopathic generalized, susceptibility to, 5
|
12760 |
|
|
epilepsy, idiopathic generalized, susceptibility to, 5; EIG5
|
http://purl.obolibrary.org/obo/MONDO_0012760 |
|
