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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
mental retardation, autosomal recessive 34; MRT34 http://purl.obolibrary.org/obo/MONDO_0013785
intellectual disability, autosomal recessive type 34 13785
mental retardation, autosomal recessive type 34 13785
congenital, autosomal dominant nystagmus 2 C537854
familial nuchal bleb C537852
White blood cell decreased 3785
nystagmus 1, congenital, x- linked C537853
nystagmus 1, congenital, x-linked C537853
congenital nystagmus, corneal pannus, and presenile cataracts foveal hypoplasia C537858
congenital, autosomal dominant nystagmus 3 C537855
congenital, autosomal dominant nystagmus 4 C537856
familial, 2, due to red cell leak pseudohyperkalemia C563785
autosomal recessive non-syndromic intellectual disability caused by mutation in CRADD 13785
presenile cataract foveal hypoplasia C537858
fetal cystic hygroma C537852