Phenotypes for disease #03016 (CMT4J (Charcot-Marie-Tooth disease, type 4J (CMT-4J)), OMIM:611228)

7 entries on 1 page. Showing entries 1 - 7.
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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     
0000060870 - - - Unknown - - - - - Gemeinschaftspraxis für Humangenetik Dresden 00081290
0000326472 Gait disturbance HP:0001288 Achilles tendon contracture HP:0001771 Pes cavus HP:0001761 Lower limb amyotrophy HP:0007210 Lower limb muscle weakness HP:0007340 Areflexia HP:0001284 Impaired tactile sensation HP:0010830 Distal upper limb amyotrophy HP:0007149 Upper limb muscle weakness HP:0003484 Demyelinating peripheral neuropathy HP:0007108 Sensorimotor neuropathy HP:0007141 Parkinsonism HP:0001300 - CMT4J with parkinsonism Familial, autosomal recessive 60y - 10y-20y Gait disturbance HP:0001288, Achilles tendon contracture HP:0001771 - Barbora Lauerova 00436292
0000326525 Gait disturbance HP:0001288 Impaired tactile sensation HP:0010830 Lower limb muscle weakness HP:0007340 Lower limb amyotrophy HP:0007210 Upper limb muscle weakness HP:0003484 Demyelinating peripheral neuropathy HP:0007108 Sensorimotor neuropathy HP:0007141 Parkinsonism HP:0001300 Foot deformity HP:0001760 - CMT4J with parkinsonism Familial, autosomal recessive 70y - - - - Barbora Lauerova 00436346
0000326526 Pes cavus HP:0001761 Lower limb muscle weakness HP:0007340 Areflexia HP:0001284 Distal upper limb amyotrophy HP:0007149 Upper limb muscle weakness HP:0003484 Gait disturbance HP:0001288 Demyelinating peripheral neuropathy HP:0007108 Sensorimotor neuropathy HP:0007141 - CMT4J with parkinsonism Familial, autosomal recessive 50y - <10y - - Barbora Lauerova 00436347
0000330577 HP:0008947; HP:0001263; HP:0001249; HP:0001284; HP:0001266; HP:0000407; HP:0001271 hypotonia, global developmental delay, areflexia, dysmorphic features CMT4J Familial, autosomal recessive 02y 05y 02y? - - Guillermo Lay-Son 00441138
0000330578 HP:0001271; HP:0006855 hypotonia, global developmental delay, areflexia, dysmorphic features SCAR20 Familial, autosomal recessive 02y 05y 02y? - - Guillermo Lay-Son 00441138
0000337703 Pes cavus HP:0001761 Lower limb muscle weakness HP:0007340 Areflexia HP:0001284 Distal upper limb amyotrophy HP:0007149 Upper limb muscle weakness HP:0003484 Gait disturbance HP:0001288 Demyelinating peripheral neuropathy HP:0007108 Sensorimotor neuropathy HP:0007141 - CMT4J with parkinsonism Familial, autosomal recessive - - <10y - - Barbora Lauerova 00448528
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