MONDO_merge Find_IDs Find_Terms Annotation
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created at 2021-12-22 03:08:20 UTC
updated at 2021-12-22 07:06:09 UTC
MONDO_bioport_pref_name
183,974 entries
Label
Id
marfanoid habitus and specific language and learning disabilities C567864
syndrome, CACH VWM D056784
oligodactylous clubfeet, and anonychia-nail hypoplasia syndrome fibular agenesis-hypoplasia C567819
diffusa, myelinosis centralis D056784
primary, 3 biliary cirrhosis C567816
primary, 2 biliary cirrhosis C567817
XP, group c C567886
complementation group c xeroderma pigmentosum C567886
myopathy, myofibrillar, bag3-related C567843
diffusas, myelinosis centralis D056784
developmental delay, coarse facies, and early death growth retardation C567856
xeroderma pigmentosum, complementation group c C567886
dilated, 1BB cardiomyopathy C567877
growth retardation, cataract, hearing loss, and unusual appearance microcephaly C567849
myelinosis centralis diffusas D056784