autosomal recessive disease
(Q10267817)
genetic disease characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop
genetic disease characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop
Language:
Current Data About
autosomal recessive disease
(P31) |
(Q112193867)
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(P279) |
(Q18553442)
(Q12136) |
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(P373) |
Autosomal recessive diseases
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(P828) |
(Q15729064)
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(P910) |
(Q6902466)
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(P1199) |
(Q15729064)
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(P1692) |
758.5
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(P2888) |
http://purl.obolibrary.org/obo/DOID_0050737
http://identifiers.org/doid/DOID:0050737
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(P5008) |
(Q4099686)
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other details
aliases |
autosomal recessive hereditary disease autosomal recessive hereditary disorder autosomal recessive inherited disorder autosomal recessive inherited disease disease, autosomal recessive recessive hereditary disorder (autosomal) |
description | genetic disease characterized by the presence of two mutated copies of the gene, both of which must be present in order for the disease or trait to develop |
External Links
(P699) |
DOID:0050737
|
(P2671) |
/g/1239cv4p
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(P5270) |
MONDO_0006025
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(P11956) |
1000017
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