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Mondo Disease Ontology
MONDO
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Label
Id
Description
obsolete parotid gland adenoid cystic carcinoma
MONDO_0000546
spondyloarthropathy
MONDO_0005095
sublingual gland adenoid cystic carcinoma
MONDO_0000545
sublingual gland carcinoma
MONDO_0021070
ovarian melanoma
MONDO_0000543
metastatic melanoma
MONDO_0005191
Gaucher disease due to saposin C deficiency
MONDO_0012517
congenital myasthenic syndrome 12
MONDO_0012518
glaucoma 1, open angle, M
MONDO_0012515
mandibulofacial dysostosis-microcephaly syndrome
MONDO_0012516
Rubinstein-Taybi syndrome due to 16p13.3 microdeletion
MONDO_0012519
chromosome 16p13.3 deletion syndrome
MONDO_0022752
xeroderma pigmentosum group B
MONDO_0012531
hereditary hemorrhagic telangiectasia type 4
MONDO_0012532
palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome
MONDO_0012530
holoprosencephaly, recurrent infections, and monocytosis
MONDO_0012535
osteogenesis imperfecta type 7
MONDO_0012536
autism, susceptibility to, 7
MONDO_0012533
combined oxidative phosphorylation defect type 4
MONDO_0012534
cervical neuroblastoma
MONDO_0000549