Phenotypes for disease #03624 (EMPF (encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF)))

9 entries on 1 page. Showing entries 1 - 9.
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Individual ID     
0000054295 - - - Familial, autosomal dominant - - - - - NeuroMeGen 00074478
0000060611 Encephalopahty, lethal, due to defective m peroxisomal fission (OMIM:614388) - - Isolated (sporadic) - - - - - Daniel Trujillano 00081042
0000078998 see paper; microcephaly (HP:0000252), abnormal brain development (HP:0012443), optic atrophy (HP:0000648), optic hypoplasia (HP:0000609), persistent lactic acidemia (HP:0003128), mildly elevated plasma concentration of very-long-chain fatty acids (HP:0003455), ... - - Isolated (sporadic) - - 00y00m00d - - Johan den Dunnen 00100785
0000078999 see paper; chronic neurological disorder, postnatal microcephaly, developmental delay, pain insensitivity; muscle biopsy disclosed decreased respirato ry chain complex IV activity, ... - - Isolated (sporadic) - - 00y06m developmental delay - Johan den Dunnen 00100786
0000079000 see paper; born from twin pregnancy 2nd twin died at 21w; 36w delivered by cesarean for non-reassuring fetal heart rate, ... - - Familial, autosomal recessive - - - - - Johan den Dunnen 00100787
0000079001 see paper; 37w cesarean due to fetal distress; birth profoundly hypotonic with absent respiratory effort required intubation and cardiopulmonary resuscitation for 12 minutes, ... - - Familial, autosomal recessive - - <00y00m00d - - Johan den Dunnen 00100788
0000166520 - - EMPF-1 Isolated (sporadic) - - - - - Daniela Verrigni 00218065
0000166521 - - EMPF-1 Isolated (sporadic) - - - - - Daniela Verrigni 00218066
0000166522 - - EMPF-1 Isolated (sporadic) - - - - - Daniela Verrigni 00218067
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