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Mondo Disease Ontology
MONDO
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Label
Id
Description
neurodevelopmental disorder with seizures and speech and walking impairment
MONDO_0032775
odonto-onycho dysplasia-alopecia syndrome
MONDO_0017134
hearing loss, autosomal recessive 99
MONDO_0032776
olivopontocerebellar atrophy-deafness syndrome
MONDO_0017135
hepatoerythropoietic porphyria
MONDO_0019799
porphyria cutanea tarda
MONDO_0015104
uridine-cytidineuria
MONDO_0032773
omodysplasia
MONDO_0017136
onchocerciasis
MONDO_0017137
cerebellar, ocular, craniofacial, and genital syndrome
MONDO_0032774
obsolete acute hepatic porphyria
MONDO_0019798
paragangliomas 7
MONDO_0032771
obsolete genetic urogenital tumor
MONDO_0017130
brain abnormalities, neurodegeneration, and dysosteosclerosis
MONDO_0032772
acalvaria
MONDO_0019795
hereditary ATTR amyloidosis
MONDO_0017132
obsolete genetic systemic or rheumatologic disease
MONDO_0017133
intellectual developmental disorder with severe speech and ambulation defects
MONDO_0032770
autosomal dominant cerebellar ataxia type IV
MONDO_0019794
recessive mitochondrial ataxia syndrome
MONDO_0019791