Rare Disease Library

OBSOLETE: Mitochondrial oxidative phosphorylation disorder due to a duplication of mitochondrial DNA

OBSOLETE: OXPHOS disease due to a duplication of mtDNA · OBSOLETE: OXPHOS disease due to a duplication of mitochondrial DNA

Mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mitochondrial DNA

Mitochondrial oxidative phosphorylation disorder due to a large-scale single deletion of mtDNA · OXPHOS disease due to a large-scale single deletion of mitochondrial DNA

Mitochondrial oxidative phosphorylation disorder due to a point mutation of mitochondrial DNA

Mitochondrial oxidative phosphorylation disorder due to a point mutation of mtDNA · OXPHOS disease due to a point mutation of mitochondrial DNA

Mitochondrial oxidative phosphorylation disorder due to mitochondrial DNA anomalies

Mitochondrial oxidative phosphorylation disorder due to mtDNA anomalies · OXPHOS disease due to mitochondrial DNA anomalies

Mitochondrial oxidative phosphorylation disorder due to nuclear DNA anomalies

Mitochondrial oxidative phosphorylation disorder due to nDNA anomalies · OXPHOS disease due to nDNA anomalies

OBSOLETE: Digestive duplication

OBSOLETE: Duplication 4q

OBSOLETE: Trisomy 4q

OBSOLETE: Mitochondrial disorder due to a transcription or a translation defect of mitochondrial DNA

OBSOLETE: Mitochondrial disorder due to a transcription or a translation defect of mtDNA

OBSOLETE: Rare eye disease due to a differentiation anomaly

OBSOLETE: X-linked acrogigantism due to Xq26 microduplication

OBSOLETE: X-LAG due to dup(X)q(26) · OBSOLETE: Familial infantile gigantism due to dup(X)q(26)