Phenotypes for disease #04248 (encephalomyopathy, mitochondrial)

5 entries on 1 page. Showing entries 1 - 5.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000028314 mitochondrial encephalomyopathy - - Familial, X-linked recessive - - - - - Daria Diodato 00037763
0000054238 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:?), - - Familial, autosomal recessive 19y - - lactic acidosis (HP:0003128), poor feeding (HP:0011968), irritability (HP:0000737), hepatomegaly (HP:0002240), bilateral cataracts (HP:0000519) - Jamie Zeegers 00074420
0000092375 - - - Familial, autosomal recessive - - - - - Daniele Ghezzi 00116637
0000171372 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) - - Familial, autosomal recessive 03y - 00y06m - - Thomas Foulonneau 00225634
0000242284 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) - - Familial, autosomal recessive - - - - - Le Guo 00320233
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