All terms in MONDO
| Label |
Id |
Description |
|
midline cerebral malformation
|
MONDO_0017090 |
|
|
prelingual non-syndromic genetic hearing loss
|
MONDO_0016297 |
|
|
Hernández-Aguirre Negrete syndrome
|
MONDO_0016290 |
|
|
craniosynostosis, Herrmann-Opitz type
|
MONDO_0016291 |
|
|
nodular neuronal heterotopia
|
MONDO_0016292 |
|
|
congenital alveolar dysplasia due to FGF10
|
MONDO_0100090 |
|
|
congenital alveolar dysplasia
|
MONDO_0100077 |
|
|
inherited pseudoxanthoma elasticum
|
MONDO_0100091 |
|
|
myoclonus, familial, 2
|
MONDO_0100092 |
|
|
myoclonus, familial
|
MONDO_0013981 |
|
|
myoclonus, familial, 1
|
MONDO_0100093 |
|
|
cannabinoid hyperemesis syndrome
|
MONDO_0100094 |
|
|
neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures
|
MONDO_0100095 |
|
|
congenital alveolar dysplasia due to TBX4
|
MONDO_0100097 |
|
|
dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive
|
MONDO_0100098 |
|
|
dopa-responsive dystonia
|
MONDO_0016812 |
|
|
retrograde cricopharyngeus dysfunction
|
MONDO_0100099 |
|
|
ankle injury
|
MONDO_0043895 |
|
|
prosthesis-related infectious disease
|
MONDO_0043892 |
|
|
autism, susceptibility to, 14a
|
MONDO_0800275 |
|
