Phenotypes for disease #05163 (mitochondrial respiratory chain deficiency)

14 entries on 1 page. Showing entries 1 - 14.
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Age/Examination     

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Age/Onset     

Phenotype/Onset     

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Individual ID     
0000050916 see paper; ..., myopathy, hypotonia, sensorineural deafness, liver involvement; elevated serum and CSF lactate levels; COX-deficient, ragged-red fibers; deceased from respiratory failure - - Familial, autosomal recessive - - 00y00m01d lactic acidosis, hypotonia, feeding difficulties, deafness - Johan den Dunnen 00064757
0000050917 see paper; ..., hypotonia, deafness; elevated serum, urine, and CSF lactate levels; deceased respiratory failure - - Familial, autosomal recessive - - 00y00m01d lactic acidosis, hypotonia, feeding difficulties, deafness - Johan den Dunnen 00064758
0000061149 see paper; ... - - Familial, autosomal recessive 04y - - - - Isabelle Thiffault 00081477
0000061150 see paper; ... - - Familial, autosomal recessive 09y - - - - Isabelle Thiffault 00081478
0000061151 see paper; ... - - Familial, autosomal recessive - - - - - Isabelle Thiffault 00081479
0000070142 Encephalopathy, seizures, microcephaly. - - Familial, autosomal recessive 10y 08y 03y - - Mark Tarnopolsky 00091700
0000082843 Leigh syndrome - - Familial, autosomal recessive - - - - - Fabian Baertling 00104960
0000092441 - - - Unknown - - - - - Fabian Baertling 00117195
0000153014 Leigh Syndrome (MIM 256000) Mitochondrial complex IV deficiency - - Familial, autosomal recessive - - 00y04m - - Sze Chern Lim 00204777
0000362744 9m-deceased; muscular hypotonia; rotary nystagmus; immunodeficiency; failure to thrive; hepatopathy; atrial septum defect respiratory chain deficiency - Familial, autosomal recessive 9m - 1d - - Johan den Dunnen 00478224
0000362745 juvenile-onset slowly progressive myopathy, limb-girdle weakness respiratory chain deficiency LGMDR1 Familial, autosomal recessive 17y - 14y - - Johan den Dunnen 00478225
0000362746 axial muscle weakness; ptosis; repiratory failure (ventilation) respiratory chain deficiency CMS5 Familial, autosomal recessive 6y - 1d - - Johan den Dunnen 00478226
0000362747 9m-deceased; muscle weakness; spastic tetraparesis, psychomotor retardation;visual loss; deafness; respiratory problems;hypomethylation;cerebellar hypoplasia; thisn corpus callosum respiratory chain deficiency PCH1C Familial, autosomal recessive 9m - 2m - - Johan den Dunnen 00478227
0000362748 cerebellar ataxia; cerebellar atrophy; dysarthria, intellectual diability;seizures; saccadic pursuit respiratory chain deficiency SCAR10 Familial, autosomal recessive 57y - 5y - - Johan den Dunnen 00478228
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