Phenotypes for disease #01926 (MEOAL;MMDS8 (mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy), OMIM:251900)

43 entries on 1 page. Showing entries 1 - 43.
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Individual ID     
0000020184 myopathy characterized by proximal muscle weakness, severe amyotrophy, excessive fatigability, dysarthria, paresis of facial muscles and ptosis - - Familial, autosomal recessive >34y - - - - Arnaud Vanlander 00022414
0000028014 severe congenital muscular hypotonia - - Isolated (sporadic) - - - - - Sander Pajusalu 00037522
0000066759 see paper; ..., congenital myopathy, ataxia, skeletal abnormalities, Cesarean section due tonon-reassuring fetal status, slight neonatal asphyxia (Apgar score 5/7), intact in first months after birth; severe growth delay, severe motor delay; severe growth impairment (<3rd percentile); no intellectual disability; no seizure; muscle weakness; tremor; dysmetry; adiadochokinesia; walking disturbance; pgmentary retinopathy, papillary pallor; triangular face, sunken eyes, chest asymmetry; raised CK (1200U/L); muscle biopsy myopathic; MRI global cerebellar hypotrophy, enlarged cisterna magna, hyperintense signals in the supra-tentorial periventricular and posterior white matter - MMYAT Familial, autosomal recessive 16y - <00y09m - - Daniele Ghezzi 00087232
0000156011 myalgia (belastungsabhängig), muscle stiffness myalgia - Unknown - - - - - Andreas Laner 00035071
0000156063 myasthenia myasthenia - Unknown - - - - - Andreas Laner 00035223
0000156066 muscular hypotonia, developmental delay muscular hypotonia - Unknown - - - - - Andreas Laner 00035227
0000156067 muscular hypotonia (aggravation with heat), mild CK-increase, path. rep. stimulation of N. accessorius bilateral, muscular hypotonia - Unknown - - - - - Andreas Laner 00035229
0000156087 muscle stiffness and muscle pain muscle disease - Unknown - - - - - Andreas Laner 00035256
0000156110 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035318
0000156113 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035321
0000156115 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035323
0000156118 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035327
0000156119 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035328
0000156120 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035329
0000156121 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035330
0000156122 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035331
0000156123 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035332
0000156124 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035333
0000156125 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035334
0000156126 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035335
0000156127 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035336
0000156128 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035337
0000156129 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035338
0000156130 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035340
0000156131 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035341
0000156132 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035342
0000156133 mitochondrial myopathy mitochondrial myopathy - Unknown - - - - - Andreas Laner 00035343
0000156141 Multiple hemorrhagic porencephalic brain lesions, at birth transient platelet defiency with petechiae, mild facial dysmorphism brain lesions - Unknown - - - - - Andreas Laner 00035356
0000156272 Muenke syndrome Muenke syndrome - Unknown - - - - - Andreas Laner 00035811
0000156276 mother: autosomal dominante hereditary leiomyomatosis leiomyomatosis? - Unknown - - - - - Andreas Laner 00035820
0000156339 Muscular Dystrophy, no further information muscular dystrophy - Unknown - - - - - Andreas Laner 00036041
0000156346 myalgia myalgia - Unknown - - - - - Andreas Laner 00036083
0000156408 mother: Muir-Torre syndrome Muit Torre syndrome? - Unknown - - - - - Andreas Laner 00036241
0000156688 mother healthy, result of daughter: suspected Dravet syndrome Dravet syndrome? - Unknown - - - - - Andreas Laner 00036786
0000156760 muscle disease muscle disease - Unknown - - - - - Andreas Laner 00036925
0000156765 mother: myotonia; son: muscle pain (cramps in hand- and foot muscles myotonia? - Unknown - - - - - Andreas Laner 00036931
0000156790 mitochondrial myopathy type I; succinat dehydrogenase deficiency mitochondrial myopathy - Unknown - - - - - Andreas Laner 00037009
0000156813 moderate anemia,neutropenia, bilateral sensorineural deafness, heart disease anemia - Unknown - - - - - Andreas Laner 00037098
0000156844 myasthenia, short stature, mikrocephaly, speech disorder, suspected Barth syndrome myasthenia - Unknown - - - - - Andreas Laner 00037223
0000156879 MNGIE mitochondrial DNA depletion syndrome - Unknown - - - - - Andreas Laner 00037308
0000156902 Mowat-Wilson syndrome Mowat-Wilson syndrome - Unknown - - - - - Andreas Laner 00037448
0000270395 see paper; ..., reluctance to stand and walk unsupported, speech acquisition delay; no intellectual disability; no seizure; muscle weakness; tremor; dysmetry; adiadochokinesia; walking disturbance; ophthalomology normal; tightness Achilles tendons; raised CK (5420 IU/L; 3y6m-MRI hypoplasia cerebellar vermis and hemispheres - MMYAT Familial, autosomal recessive 03y06m - 01y - - Johan den Dunnen 00375185
0000270396 see paper; ..., mitochondrial myopathy, ataxia, muscle weakness; short stature (150 cm); no seizure; adiadochokinesia; ophthalmology normal; normal CK; muscle biopsy myopathic; frontal atrophy, enlarged interhemispheric fissure - MMYAT Familial, autosomal dominant 38y - 38y - - Johan den Dunnen 00375186
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