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Mondo Disease Ontology
MONDO
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Label
Id
Description
minimal pigment oculocutaneous albinism type 1
MONDO_0018136
obsolete ocular albinism with congenital sensorineural hearing loss
MONDO_0018138
temperature-sensitive oculocutaneous albinism type 1
MONDO_0018137
obsolete congenital muscular alpha-dystroglycanopathy with brain and eye anomalies
MONDO_0018132
neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion
MONDO_0018131
neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome
MONDO_0018681
disorder of melanin metabolism
MONDO_0018134
attenuated Chédiak-Higashi syndrome
MONDO_0018133
brain dopamine-serotonin vesicular transport disease
MONDO_0018130
inborn disorder of neurotransmitter metabolism and transport
MONDO_0019219
colorectal diffuse large B-cell lymphoma
MONDO_0006158
colorectal lymphoma
MONDO_0024656
colorectal gastrointestinal stromal tumor
MONDO_0006159
colon sessile serrated adenoma/polyp
MONDO_0006156
colorectal sessile serrated adenoma/polyp
MONDO_0006164
colorectal adenosquamous carcinoma
MONDO_0006157
colon mucosa-associated lymphoid tissue lymphoma
MONDO_0006154
colorectal neuroendocrine tumor G1
MONDO_0006162
neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor
MONDO_0015067
colon inflammatory polyp
MONDO_0006152