Abnormal lower motor neuron morphology

Symptom Information:

Symptom ID: HPO:0002366
Synonyms:
Lower motor neuron disease [HPO:0002366]
Lower motor neuron manifestations [HPO:0002366]
Lower motor neuron signs [HPO:0002366]
Lower motor neuron disease [OMIM:Lower motor neuron disease]
Lower motor neuron manifestations [OMIM:Lower motor neuron manifestations]
Lower motor neuron signs [OMIM:Lower motor neuron signs]
Quality:
Cross references:
OMIM: "Lower motor neuron disease" [OMIM:Lower motor neuron disease]
OMIM: "Lower motor neuron manifestations" [OMIM:Lower motor neuron manifestations]
OMIM: "Lower motor neuron signs" [OMIM:Lower motor neuron signs]
Is a (Direct Parents):
HPO         Abnormal peripheral nervous system morphology
HPO         Abnormal motor neuron morphology
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)
             Abnormal peripheral nervous system morphology(HPO:0000759)
                Abnormal lower motor neuron morphology(HPO:0002366)
             Morphological abnormality of the central nervous system(HPO:0002011)
                Abnormal motor neuron morphology(HPO:0002450)
                   Abnormal lower motor neuron morphology(HPO:0002366)
MedDRA:
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)