All terms in MONDO
| Label |
Id |
Description |
|
hereditary cryohydrocytosis with reduced stomatin
|
MONDO_0012143 |
|
|
obsolete pulmonary function
|
MONDO_0012140 |
|
|
orofacial cleft 6, susceptibility to
|
MONDO_0012141 |
|
|
obsolete mental retardation, X-linked, nonsyndromic
|
MONDO_0000168 |
|
|
Huntington disease and related disorders
|
MONDO_0000167 |
|
|
obsolete ectodermal dysplasia-syndactyly syndrome
|
MONDO_0000165 |
|
|
microphthalmia, isolated, with cataract
|
MONDO_0000169 |
|
|
obsolete corneal dystrophy, Fuchs endothelial
|
MONDO_0000164 |
|
|
obsolete breast-ovarian cancer, familial, susceptibility to
|
MONDO_0000163 |
|
|
obsolete adrenal hyperplasia
|
MONDO_0000161 |
|
|
congenital myasthenic syndrome 4C
|
MONDO_0012157 |
|
|
keratoconus 2
|
MONDO_0012158 |
|
|
choanal atresia
|
MONDO_0012155 |
|
|
myasthenic syndrome, congenital, 1B, fast-channel
|
MONDO_0012156 |
|
|
congenital myasthenic syndrome 1A
|
MONDO_0011088 |
|
|
lung cancer susceptibility 1
|
MONDO_0012159 |
|
|
attention deficit-hyperactivity disorder, susceptibility to, 2
|
MONDO_0012150 |
|
|
Alzheimer disease 9
|
MONDO_0012153 |
|
|
myopia 6
|
MONDO_0012154 |
|
|
attention deficit-hyperactivity disorder, susceptibility to, 3
|
MONDO_0012151 |
|
