Abnormal lower motor neuron morphology
Symptom Information:
Symptom ID: | HPO:0002366 | ||||||
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 lower motor neuron morphology(HPO:0002366) Abnormal peripheral nervous system morphology(HPO:0000759) Abnormal lower motor neuron morphology(HPO:0002366) MedDRA: |
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Database Frequency: | 12 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
AMYOTROPHIC LATERAL SCLEROSIS 16, JUVENILE | (OMIM:614373) |
AMYOTROPHIC LATERAL SCLEROSIS 2, JUVENILE | (OMIM:205100) |
AMYOTROPHIC LATERAL SCLEROSIS 5 | (OMIM:602099) |
Amyotrophic lateral sclerosis type 4 | (Orphanet:357043) |
Amyotrophic lateral sclerosis-parkinsonism-dementia complex | (Orphanet:90020) |
Autosomal recessive lower motor neuron disease with childhood onset | (Orphanet:206580) |
Distal myopathy with vocal cord weakness | (Orphanet:600) |
Frontotemporal dementia with motor neuron disease | (Orphanet:275872) |
Infantile-onset ascending hereditary spastic paralysis | (Orphanet:293168) |
Juvenile amyotrophic lateral sclerosis | (Orphanet:300605) |
NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE VIIB | (OMIM:607641) |
Neurodegeneration with brain iron accumulation due to C19orf12 mutation | (Orphanet:289560) |