Disease #04248 (encephalomyopathy, mitochondrial)

Official abbreviation -
Name encephalomyopathy, mitochondrial
OMIM ID -
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2015-05-03 13:18:08 +02:00 (CEST)
Date last edited N/A


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00037763 - - - M - Italy - - - - - encephalomyopathy, mitochondrial mitochondrial encephalomyopathy AIFM1 AIFM1 1 1 Daria Diodato
00074420 - PubMed: Calderwood 2016, Journal: Calderwood 2016 No family history F - - - >19y - - - encephalomyopathy, mitochondrial adrenal insufficiency (HP:0000846), moderately cognitively delayed (HP:0001263), muscle weakness (HP:0001324), wide-based gait (HP:0002136), neck hyperextension (HP:?), truncal instability (HP:?), restrictive lung disease (HP:0002091), elevated plasma lactate levels (HP:?), GFER GFER 2 1 Jamie Zeegers
00116637 - - - F no Italy - - - - - encephalomyopathy, mitochondrial - VARS2 VARS2 2 1 Daniele Ghezzi
00225634 - PubMed: Sadat 2016 1 affected M no - Mixed Afro-Caribbean and East indian ancestry - - - - encephalomyopathy, mitochondrial Ataxia (HP:0001251); Seizures (HP:0001250); Cerebellar atrophy (HP:0001272); Aplasia/Hypoplasia of the cerebellum (HP:0007360); Profound global developmental delay (HP:0012736); Sensorineural hearing impairment (HP:0000407); Abnormal saccadic eye movements (HP:0000570); Abnormal facial shape/dysmorphic facial features (HP:0001999); Muscular hypotonia (HP:0001252); Myoclonus (HP:0001336) ACO2 ACO2 2 1 Thomas Foulonneau
00320233 - - - M no Netherlands - 00y18m - Yes - encephalomyopathy, mitochondrial Opisthotonus (HP:0002179), motor delay (HP:0001270), inspiratory stridor (HP:0005348), nystagmus (HP:0000639), tremor (HP:0001337), peripheral axonal neuropathy (HP:0003477), areflexia (HP:0001284), generalized muscle weakness (HP:0003324) - SLIRP 2 1 Le Guo
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