Phenotypes for disease #02504 (CEMCOX1 (cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1), OMIM:604377)

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0000272751 Neuromuscular disease or hereditary sensory-motor neuropathy (axonal) with paraparesis of the legs, contractures of the ankle and metacarpophalangeal joints of the thumb, atrophy of the calf and foot muscles as well as the hand muscles, tongue fasciculations, tremor of the hands, Pes cavus on both sides, loss of the ability to walk at the age of 11. Younger brother with possible onset of similar symptoms - - Familial, autosomal recessive 13y - - - - Andreas Laner 00377599
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