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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
laurence-moon-biedl syndrome D007849
syndrome, laurence-moon D007849
syndrome, laurence-moon-biedl D007849
laurence moon biedl syndrome D007849
Keratoendotheliitis fugax hereditaria 7849
keratitis fugax hereditaria 7849
KERATOENDOTHELIITIS fugax hereditaria; KEFH http://purl.obolibrary.org/obo/MONDO_0007849
fatal multisystem syndrome involving the eyes, ears, lungs, intestines, and kidneys 17849
congenital progressive oculo-acoustico-cerebral degeneration C537849
laurence moon syndrome D007849