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
postaxial polydactyly, type a4 C563909
Bartter disease type 4B 909
Bartter syndrome, type 4B 909
Bartter syndrome, type 4B, neonatal, with sensorineural deafness 909
Bartter syndrome, type 4B, neonatal, with sensorineural deafness; BARTS4B http://purl.obolibrary.org/obo/MONDO_0000909
Bartter syndrome, type 4b, digenic 909
Dermatoosteolysis Kirghizian type 9095
dermatoosteolysis, Kirghizian type 9095
UV-sensitive syndrome type 1 10909
Ring chromosome type 16 19909
persistent fetal vasculature 9097
congenital Epstein-Barr virus infection 19094
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia 9096
dextrocardia with unusual facies and microphthalmia 9098
leukoencephalopathy, adult-onset, with axonal spheroids and pigmented glia 9096