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

There is 0 pattern entry.

Label
Id
syndrome, williams D018980
syndrome, williams-beuren D018980
williams syndrome D018980
williams-beuren syndrome D018980
boucher-NEUHAUSER syndrome; BNHS http://purl.obolibrary.org/obo/MONDO_0008980
limb ischemia, critical D000089802
chromosome 7q11.23 deletion syndrome D018980
williams contiguous gene syndrome D018980
spinocerebellar ataxia, hypogonadotropic hypogonadism, and chorioretinal dystrophy 8980
chronic limb-threatening ischemia D000089802
aortic stenoses, hypercalcemia-supravalvar D018980
aortic stenosis, hypercalcemia-supravalvar D018980
ataxia - hypogonadism - choroidal dystrophy 8980
critical limb ischemia D000089802
chorioretinal dystrophy, spinocerebellar ataxia and hypogonadotropic hypogonadism 8980
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