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1
Q35070259-1C0E380C-F577-405D-A7CF-ABBDE169F4D4
Q35070259-1C0E380C-F577-405D-A7CF-ABBDE169F4D4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35070259-1C0E380C-F577-405D-A7CF-ABBDE169F4D4
Ophthalmological phenotype associated with homozygous null mutation in the NEUROD1 gene.
P2860
Q35070259-1C0E380C-F577-405D-A7CF-ABBDE169F4D4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35070259-1C0E380C-F577-405D-A7CF-ABBDE169F4D4
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
833b901d07875897408ddd8769e3812cae44386a
P2860
Homozygous mutations in NEUROD1 are responsible for a novel syndrome of permanent neonatal diabetes and neurological abnormalities.