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Up to: Hereditary disease
Autosomal genetic disease
A monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes.
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Autosomal recessive disease 4 trials · 994 incl. sub-types Sub-types →
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Autosomal dominant disease 0 trials · 699 incl. sub-types Sub-types →
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Congenital factor XII deficiency 1 trial
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Septooptic dysplasia 1 trial Sub-types →
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Weill-Marchesani syndrome 0 trials Sub-types →
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Brachydactyly-syndactyly syndrome 0 trials
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Congenital factor XI deficiency 0 trials