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Q24532090-7E48EAAF-893B-49BB-9CA7-6EA3B7EB5DC7
Q24532090-7E48EAAF-893B-49BB-9CA7-6EA3B7EB5DC7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24532090-7E48EAAF-893B-49BB-9CA7-6EA3B7EB5DC7
Homozygous mutations in IHH cause acrocapitofemoral dysplasia, an autosomal recessive disorder with cone-shaped epiphyses in hands and hips.
P2860
Q24532090-7E48EAAF-893B-49BB-9CA7-6EA3B7EB5DC7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24532090-7E48EAAF-893B-49BB-9CA7-6EA3B7EB5DC7
rank
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type
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wasDerivedFrom
ee95e03a5ca24d42babe9a54a48865cebb6d6840
P2860
Mutation of the gene encoding the ROR2 tyrosine kinase causes autosomal recessive Robinow syndrome