Abnormal upper motor neuron morphology
Symptom Information:
Symptom ID: | HPO:0002127 | ||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the nervous system(HPO:0000707) Abnormality of nervous system morphology(HPO:0012639) Morphological abnormality of the central nervous system(HPO:0002011) Abnormal motor neuron morphology(HPO:0002450) Abnormal upper motor neuron morphology(HPO:0002127) MedDRA: |
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Database Frequency: | 15 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE | (OMIM:614373) |
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE | (OMIM:205100) |
Adult polyglucosan body disease | (Orphanet:206583) |
Amyotrophic lateral sclerosis type 4 | (Orphanet:357043) |
Ataxia - hypogonadism - choroidal dystrophy | (Orphanet:1180) |
Autosomal dominant spastic paraplegia type 9 | (Orphanet:100990) |
Distal myopathy with vocal cord weakness | (Orphanet:600) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
Juvenile primary lateral sclerosis | (Orphanet:247604) |
Leukoencephalopathy - ataxia - hypodontia - hypomyelination | (Orphanet:137639) |
NEUROPATHY, HEREDITARY SENSORIMOTOR, WITH UPPER MOTOR NEURON, VISUALPATHWAY AND AUTONOMIC DISTURBANCE | (OMIM:162380) |
Nasu-Hakola disease | (Orphanet:2770) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |
Odontoleukodystrophy | (Orphanet:77295) |
Primary lateral sclerosis | (Orphanet:35689) |