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Mondo Disease Ontology
MONDO
All terms in MONDO
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Label
Id
Description
Ehlers-Danlos syndrome, musculocontractural type
MONDO_0011142
chromosome 22q13 duplication syndrome
MONDO_0014235
reticulate acropigmentation of Kitamura
MONDO_0014234
obsolete partial deletion of the short arm of chromosome 18
MONDO_0016896
testicular anomalies with or without congenital heart disease
MONDO_0014239
severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome
MONDO_0014238
partial deletion of the short arm of chromosome 10
MONDO_0016892
obsolete partial monosomy of the short arm of chromosome 17
MONDO_0016895
early-onset Parkinson disease 20
MONDO_0014233
craniosynostosis 5, susceptibility to
MONDO_0014232
juvenile onset Parkinson disease 19A
MONDO_0014231
obsolete partial deletion of the short arm of chromosome 9
MONDO_0016891
candidiasis, familial, 8
MONDO_0014230
obsolete genetic respiratory malformation
MONDO_0026203
hypertrophic elongation of cervix
MONDO_0002255
obsolete genetic polyendocrinopathy
MONDO_0026209
ankylosis
MONDO_0002257
obsolete genetic frontotemporal degeneration with dementia
MONDO_0028868
granulomatous hepatitis
MONDO_0002252
spondylosis
MONDO_0002253