Phenotypes for disease #05403 (MRT53;GPIBD13 (mental retardation, autosomal recessive, type 53 (MRT-53, glycosylphosphatidylinositol deficiency, type 13 (GPIBD-13))), OMIM:616917)

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AscendingPhenotype ID     

Diagnosis/Initial     

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Phenotype details     

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Age/Diagnosis     

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Individual ID     
0000352724 Peripheral nerve hyperexcitability - Myokymia (HP:0002411), Gait ataxia (HP:0002066), Peripheral nerve hyperexcitability (HP:0034351), Demyelinating motor neuropathy (HP:0007220), Muscle hypertrophy of the lower extremities (HP:0008968), EMG: myokymic discharges (HP:0100288), Febrile seizure (HP:0002373) Familial, autosomal recessive 20y 27y 08y Myokymia (HP:0002411) - Pedro Henrique Marte de Arruda Sampaio 00467516
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