All terms in MONDO
| Label |
Id |
Description |
|
Weill-Marchesani syndrome 2, dominant
|
MONDO_0012013 |
|
|
maturity-onset diabetes of the young type 14
|
MONDO_0014674 |
|
|
myopathy, myosin storage, autosomal dominant
|
MONDO_0012018 |
|
|
spondyloepiphyseal dysplasia, Kimberley type
|
MONDO_0012019 |
|
|
polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis
|
MONDO_0014679 |
|
|
bilateral perisylvian polymicrogyria
|
MONDO_0020340 |
|
|
capillary malformation-arteriovenous malformation syndrome
|
MONDO_0012016 |
|
|
obsolete Parkes Weber syndrome
|
MONDO_0012017 |
|
|
intellectual disability, autosomal dominant 39
|
MONDO_0014678 |
|
|
cataract 44
|
MONDO_0014673 |
|
|
coronary heart disease, susceptibility to, 4
|
MONDO_0012010 |
|
|
coronary artery disease, autosomal dominant, 1
|
MONDO_0012011 |
|
|
osteogenesis imperfecta type 17
|
MONDO_0014672 |
|
|
neuropathy, hereditary motor and sensory, type 6B
|
MONDO_0014671 |
|
|
hereditary motor and sensory neuropathy type 6
|
MONDO_0019551 |
|
|
lethal congenital contracture syndrome 9
|
MONDO_0014670 |
|
|
obsolete pancreatic ductal carcinoma
|
MONDO_0002699 |
|
|
obsolete hemolytic anemia, nonspherocytic
|
MONDO_0000036 |
|
|
obsolete glucocorticoid deficiency
|
MONDO_0000035 |
|
|
obsolete glomerulopathy with fibronectin deposits
|
MONDO_0000034 |
|
