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1
Q52621434-2A33252B-AF17-46F2-965A-AA7ABA09DD60
Q52621434-2A33252B-AF17-46F2-965A-AA7ABA09DD60
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52621434-2A33252B-AF17-46F2-965A-AA7ABA09DD60
Phenotypic variability in hyperphosphatasia with seizures and neurologic deficit (Mabry syndrome).
P2860
Q52621434-2A33252B-AF17-46F2-965A-AA7ABA09DD60
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52621434-2A33252B-AF17-46F2-965A-AA7ABA09DD60
rank
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type
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Statement
wasDerivedFrom
2227a00858b54a35d1a4a1c73025b1710aa27b0e
P2860
Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN.