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Q34431404-F8FBD177-41A2-4E00-98A9-3AB73FF78FF9
Q34431404-F8FBD177-41A2-4E00-98A9-3AB73FF78FF9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34431404-F8FBD177-41A2-4E00-98A9-3AB73FF78FF9
Inherited bone marrow failure associated with germline mutation of ACD, the gene encoding telomere protein TPP1.
P2860
Q34431404-F8FBD177-41A2-4E00-98A9-3AB73FF78FF9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34431404-F8FBD177-41A2-4E00-98A9-3AB73FF78FF9
rank
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type
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Statement
wasDerivedFrom
472ddb207643e8eb67a4cc3ee6b99477e6caaf64
P2860
Constitutional mutations in RTEL1 cause severe dyskeratosis congenita