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Q54963859-0D9EF01C-9F5A-4CE5-B57E-96409E17BE68
Q54963859-0D9EF01C-9F5A-4CE5-B57E-96409E17BE68
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-0D9EF01C-9F5A-4CE5-B57E-96409E17BE68
A homozygous loss-of-function CAMK2A mutation causes growth delay, frequent seizures and severe intellectual disability.
P2860
Q54963859-0D9EF01C-9F5A-4CE5-B57E-96409E17BE68
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54963859-0D9EF01C-9F5A-4CE5-B57E-96409E17BE68
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
b808c7a781c26a8bfd4ec59ed2924d24834c5d84
P2860
Practice parameter: evaluation of the child with global developmental delay: report of the Quality Standards Subcommittee of the American Academy of Neurology and The Practice Committee of the Child Neurology Society.