Holt-Oram syndrome
(Q182005)
autosomal dominant disease characterized by congenital anomalies located_in heart and located_in upper limb.
autosomal dominant disease characterized by congenital anomalies located_in heart and located_in upper limb.
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Current Data About
Holt-Oram syndrome
| (P31) |
(Q55788864)
(Q929833) (Q112193867) |
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| (P138) |
(Q6779785)
(Q112515385) |
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| (P279) |
(Q18553439)
(Q18018497) (Q55785290)
(Q55785258)
(Q55785518)
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| (P1692) |
759.89
|
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| (P1748) |
C125592
|
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| (P1995) |
(Q1071953)
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| (P2293) |
(Q18031853)
|
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| (P2888) |
http://purl.obolibrary.org/obo/DOID_0060468
http://identifiers.org/doid/DOID:0060468
http://www.orpha.net/ORDO/Orphanet_392 |
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| (P5008) |
(Q4099686)
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other details
| aliases |
heart-hand syndrome atrio-digital syndrome type 1 atriodigital dysplasia type 1 atrio-digital syndrome atriodigital dysplasia Hos1 Heart-hand syndrome type 1 HOLT-ORAM SYNDROME; HOS HOS HOLT-ORAM SYNDROME Holt–Oram syndrome |
| description | autosomal dominant disease characterized by congenital anomalies located_in heart and located_in upper limb. |
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