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Q54378630-0EE6DF15-ABFE-4E80-8E4A-C7B95BDAE32C
Q54378630-0EE6DF15-ABFE-4E80-8E4A-C7B95BDAE32C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54378630-0EE6DF15-ABFE-4E80-8E4A-C7B95BDAE32C
HPPD: A newly recognized autosomal dominant disorder involving hypertelorism, preauricular sinus, punctal pits, and deafness mapping to chromosome 14q31.
P2860
Q54378630-0EE6DF15-ABFE-4E80-8E4A-C7B95BDAE32C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q54378630-0EE6DF15-ABFE-4E80-8E4A-C7B95BDAE32C
rank
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Statement
wasDerivedFrom
a711ec4b34cad9ced824d939d45cc1c5a0b10d0c
P2860
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes