Axenfeld-Rieger syndrome
(Q474994)
autosomal dominant disease characterized by abnormalities of the front part of the eye, the anterior segment
autosomal dominant disease characterized by abnormalities of the front part of the eye, the anterior segment
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Current Data About
Axenfeld-Rieger syndrome
(P31) |
(Q112193867)
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(P279) |
(Q18553439)
(Q3041498)
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(P373) |
Axenfeld syndrome
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(P1748) |
C131001
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(P1995) |
(Q1071953)
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(P2888) |
http://purl.obolibrary.org/obo/DOID_14686
http://identifiers.org/doid/DOID:14686
http://purl.obolibrary.org/obo/HP_0000558
http://www.orpha.net/ORDO/Orphanet_782 |
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(P5008) |
(Q4099686)
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other details
aliases |
Anomaly, Rieger's Axenfeld syndrome RGS - Rieger syndrome Rieger's anomaly Hagedoom syndrome |
description | autosomal dominant disease characterized by abnormalities of the front part of the eye, the anterior segment |
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