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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Tibial aplasia-ectrodactyly syndrome
Split-hand/foot malformation with long bone deficiency 2
rare
Identifiers
MONDO:0012537
OMIM:610685
Part of
Tibial aplasia-ectrodactyly syndrome
Also known as
SHFLD2
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