autosomal genetic disease
(Q18553442)
monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes
monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes
Language:
Current Data About
autosomal genetic disease
(P31) |
(Q112193867)
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(P279) |
(Q1225194)
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(P373) |
Autosomal diseases
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(P1692) |
758.5
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(P2888) |
http://purl.obolibrary.org/obo/DOID_0050739
http://identifiers.org/doid/DOID:0050739
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(P5008) |
(Q4099686)
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other details
aliases |
autosomal inherited disorder autosomal hereditary disorder autosomal inherited disease |
description | monogenic disease that is has material basis in a mutation in a single gene on one of the non-sex chromosomes |
External Links
(P699) |
DOID:0050739
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(P5270) |
MONDO_0000429
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