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Mondo Disease Ontology
MONDO
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Label
Id
Description
mirror movements 1 and/or agenesis of the corpus callosum
MONDO_0100515
familial congenital mirror movements
MONDO_0016558
hypomyelination with brain stem and spinal cord involvement and leg spasticity
MONDO_0014115
complex neurodevelopmental disorder
MONDO_0100038
cardiofaciocutaneous syndrome 4
MONDO_0014114
cardiofaciocutaneous syndrome
MONDO_0015280
PSAP-related sphingolipidosis
MONDO_0100517
cardiofaciocutaneous syndrome 3
MONDO_0014113
hereditary attention deficit-hyperactivity disorder
MONDO_0100518
attention deficit-hyperactivity disorder
MONDO_0007743
lichen planus pemphigoides
MONDO_0016775
intellectual disability-strabismus syndrome
MONDO_0014119
frontal fibrosing alopecia
MONDO_0016776
congenital neutropenia-myelofibrosis-nephromegaly syndrome
MONDO_0014118
inhalational botulism
MONDO_0016777
botulism
MONDO_0005498
iatrogenic botulism
MONDO_0016778
Charcot-Marie-Tooth disease type 4B3
MONDO_0014117
annular atrophic lichen planus
MONDO_0016771
annular lichen planus
MONDO_0016772