Phenotypic features of human mitochondrial diseases.
收藏Figshare2015-12-02 更新2026-05-11 收录
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The 144 features are selected from a total of 502 features (Table S2) and are caused by defects in 174 nuclear-encoded mitochondrial genes. Every feature is associated with the number of genes shown in parentheses. The hierarchical structure of features within the phenotype ontology was established using standardized MeSH descriptors (not shown). The fourteen CC in bold serve as headers for features within them. Unassigned features are grouped under ��Miscellaneous��.
创建时间：
2015-12-02
