Phenotypes for disease #00370 (CMT4C (Charcot-Marie-Tooth disease, type 4C (CMT-4C)), OMIM:601596)

5 entries on 1 page. Showing entries 1 - 5.
Legend   How to query  

AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000155389 sensori-motor demyelinating neuropathy in the lower limbs, scoliosis - - Familial, autosomal recessive - 29y 06y ? SH3TC2 Justine Lerat 00207578
0000291750 Demyelinating peripheral neuropathy (HP:0007108), Decreased nerve conduction velocity (HP:0000762) CMT CMT4C Familial, autosomal recessive 45y - 20y Demyelinating peripheral neuropathy (HP:0007108), Decreased nerve conduction velocity (HP:0000762) - Yvet den Hartog 00398667
0000296572 Progressive weakness and wasting of the four limbs. Bilateral foot drop. Nerve conduction velocity study showed severe demyelinating peripheral neuropathy Autosomal recessive Hereditary sensorimotor neuropathy CMT-4C Familial, autosomal recessive 28y 24y 06y - - Sherifa Ahmed Hamed 00403899
0000296573 Progressive weakness and wasting of both upper and lower limbs. severe deep sensory loss, Pes Cavus. nerve conduction velocity study showed demyelinating peripheral neuropathy. Autosomal recessive Hereditary sensorimotor neuropathy CMT-4C Familial, autosomal recessive 42y 28y 24y - - Sherifa Ahmed Hamed 00403900
0000296574 kyphoscliosis early in childhood. progressive weakness and wasting of upper and lower limbs, marked in lower limbs. Pes Cavus nerve conduction velocity study showed demyelinating sensory neurpathy Autosomal recessive Hereditary sensorimotor neuropathy CMT-4C Familial, autosomal recessive 48y 32y 28y - - Sherifa Ahmed Hamed 00403906
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.