Phenotypes for disease #05157 (HMSN (neuropathy, motor and sensory, hereditary (HMSN)))

8 entries on 1 page. Showing entries 1 - 8.
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     
0000050357 - - - Unknown - - - - - Johan den Dunnen 00063774
0000117830 - neuropathy, motor and sensory, hereditary (HMSN) HMSN Unknown - - - - - Johan den Dunnen 00145090
0000124268 - hereditary motor & sensory neuropathy - Unknown - - - - - Johan den Dunnen 00151905
0000124283 - hereditary motor & sensory neuropathy - Unknown - - - - - Johan den Dunnen 00151920
0000311843 - progressive polyneuropathy - Unknown - - - - - Gemeinschaftspraxis für Humangenetik Dresden 00420595
0000325345 - - - Unknown - - - - - Gemeinschaftspraxis für Humangenetik Dresden 00435111
0000325347 - - - Familial, autosomal dominant - - - - - Gemeinschaftspraxis für Humangenetik Dresden 00435114
0000358776 Hypotonia since 5-mo; Febrile seizures 2.5y, Delayed walking; Facial muscle weakness; Generalized muscle weakness & atrophy, lower & upper; Scoliosis; Steppage gait; Foot drop; Areflexia; Wheelchair bound; Echocardiography: mild MVP & TR; EMG-NCV: demyelinating sensorimotor peripheral neuropathy; Mildly abnormal EEG. hereditary motor and sensory neuropathy - Unknown 18y - - - - Johan den Dunnen 00473981
Legend   How to query  


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