Abnormal upper motor neuron morphology

Symptom Information:

Symptom ID: HPO:0002127
Synonyms:
Upper motor neuron disorder [HPO:0002127]
Upper motor neuron signs [HPO:0002127]
Upper motor neuron disorder [OMIM:Upper motor neuron disorder]
Upper motor neuron signs [OMIM:Upper motor neuron signs]
Quality:
Cross references:
OMIM: "Upper motor neuron disorder" [OMIM:Upper motor neuron disorder]
OMIM: "Upper motor neuron signs" [OMIM:Upper motor neuron signs]
Is a (Direct Parents):
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)
             Morphological abnormality of the central nervous system(HPO:0002011)
                Abnormal motor neuron morphology(HPO:0002450)
                   Abnormal upper motor neuron morphology(HPO:0002127)
MedDRA:
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)