WERNER SYNDROME
WRN
http://purl.bioontology.org/ontology/OMIM/277700
C0043119
8p12-p11.2
RECQ3
RECQL2
http://purl.bioontology.org/ontology/OMIM/MTHU000132
http://purl.bioontology.org/ontology/OMIM/MTHU008749
http://purl.bioontology.org/ontology/OMIM/MTHU008743
http://purl.bioontology.org/ontology/OMIM/MTHU008747
http://purl.bioontology.org/ontology/OMIM/MTHU000581
http://purl.bioontology.org/ontology/OMIM/MTHU008745
http://purl.bioontology.org/ontology/OMIM/MTHU008741
http://purl.bioontology.org/ontology/OMIM/MTHU008751
http://purl.bioontology.org/ontology/OMIM/MTHU036798
http://purl.bioontology.org/ontology/OMIM/MTHU000145
http://purl.bioontology.org/ontology/OMIM/MTHU002380
http://purl.bioontology.org/ontology/OMIM/MTHU000155
http://purl.bioontology.org/ontology/OMIM/MTHU008740
http://purl.bioontology.org/ontology/OMIM/MTHU008746
http://purl.bioontology.org/ontology/OMIM/MTHU008744
http://purl.bioontology.org/ontology/OMIM/MTHU008742
http://purl.bioontology.org/ontology/OMIM/MTHU004856
http://purl.bioontology.org/ontology/OMIM/MTHU008752
http://purl.bioontology.org/ontology/OMIM/MTHU008748
http://purl.bioontology.org/ontology/OMIM/MTHU008750
Phenotype description, molecular basis known.
277700
3
pound
Caused by mutation in the RecQ protein-like 2 gene (RECQL2, 604611.0001) [MOLECULAR BASIS]
T047