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
BFNS1 7365
seizures, benign familial neonatal, 1 7365
ichthyosis, bilateral cryptorchidism, hypogenitalism and mental retardation C537365
seizures, benign familial neonatal, 1, and/or myokymia 7365
seizures, benign familial neonatal, 1; BFNS1 http://purl.obolibrary.org/obo/MONDO_0007365
seizures, benign familial neonatal, type 1 7365
congenital poikiloderma with bullae, Weary type 17365
bilateral cryptorchidism, hypogenitalism and mental retardation ichthyosis C537365
KCNQ2 benign neonatal seizures 7365
epilepsy, benign neonatal, 1, and/or myokymia 7365
type 6 meckel syndrome C567365
hereditary acrokeratotic poikiloderma, Weary type 17365
benign neonatal seizures caused by mutation in KCNQ2 7365
meckel syndrome, type 6 C567365