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Mondo Disease Ontology
MONDO
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Label
Id
Description
neuronal ceroid lipofuscinosis 13
MONDO_0014147
autosomal dominant hypocalcemia 2
MONDO_0014146
muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14
MONDO_0014141
muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14
MONDO_0014140
muscle-eye-brain disease
MONDO_0018939
Leber congenital amaurosis 17
MONDO_0014145
autosomal recessive limb-girdle muscular dystrophy type R18
MONDO_0014144
autosomal recessive limb-girdle muscular dystrophy
MONDO_0015152
Noonan syndrome 8
MONDO_0014143
autosomal recessive limb-girdle muscular dystrophy type 2T
MONDO_0014142
muscular dystrophy-dystroglycanopathy, type C
MONDO_0000173
rectum neuroendocrine neoplasm
MONDO_0003646
digestive system melanoma
MONDO_0045070
rectum sarcoma
MONDO_0002168
rectum adenocarcinoma
MONDO_0002169
thymus lipoma
MONDO_0002163
focal chorioretinitis
MONDO_0002164
chorioretinitis
MONDO_0004674
rectum lymphoma
MONDO_0002166
obsolete cerebral palsy
MONDO_0002160