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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
acrocephalosyndactyly type V 7043
Pfeiffer type acrocephalosyndactyly 7043
ocular, with late-onset sensorineural deafness albinism C537043
waardenburg syndrome, type ii, with ocular albinism, autosomal recessive C537043
congenital mesoblastic nephroma 17043
ocular, with sensorineural deafness albinism C537043
type ii, with ocular albinism, autosomal recessive waardenburg syndrome C537043