Phenotypes for disease #01090 (HSN2C (neuropathy, sensory, hereditary, type IIC (HSN-2C)), OMIM:614213)

9 entries on 1 page. Showing entries 1 - 9.
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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     
0000086055 hereditary sensory and autonomic neuropathy - - Familial, autosomal recessive - - - - - Johan den Dunnen 00108459
0000086056 hereditary sensory and autonomic neuropathy - - Familial, autosomal recessive - - - - - Johan den Dunnen 00108460
0000086057 hereditary sensory and autonomic neuropathy - - Familial, autosomal recessive - - - - - Johan den Dunnen 00108461
0000086058 hereditary sensory and autonomic neuropathy - - Familial, autosomal recessive - - - - - Johan den Dunnen 00108462
0000086059 hereditary sensory and autonomic neuropathy - - Familial, autosomal recessive - - - - - Johan den Dunnen 00108463
0000086060 hereditary sensory and autonomic neuropathy - - Familial, autosomal recessive - - - - - Johan den Dunnen 00108464
0000086061 hereditary sensory and autonomic neuropathy - - Familial, autosomal recessive - - - - - Johan den Dunnen 00108465
0000086062 hereditary sensory and autonomic neuropathy - - Familial, autosomal recessive - - - - - Johan den Dunnen 00108466
0000291702 Peripheral neuropathy (HP:0009830), Distal muscle weakness (HP:0002460), Hearing impairment (HP:0000365), Decreased nerve conduction velocity (HP:0000762), Upper motor neuron dysfunction (HP:0002493) CMT HSN2C Familial, autosomal recessive 67y - 45y Peripheral neuropathy (HP:0009830), Distal muscle weakness (HP:0002460), Hearing impairment (HP:0000365), Decreased nerve conduction velocity (HP:0000762), Upper motor neuron dysfunction (HP:0002493) - Yvet den Hartog 00398615
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