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
CAPOS 11038
CAPOS syndrome 11038
congenitale, poikiloderma D011038
congenitales, poikiloderma D011038
poikiloderma congenitales D011038
rothmund-thomson poikiloderma D011038
rothmund-thomson poikilodermas D011038
rothmund-thomson syndrome D011038
syndrome, rothmund-thomson D011038
cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss 11038
cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome 11038
poikiloderma congenitale of rothmund-thomson D011038
rothmund thomson syndrome D011038
cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss 11038
cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss 11038