Degeneration of anterior horn cells
Symptom Information:
Symptom ID: | HPO:0002398 | ||||||||||||
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) Motor neuron atrophy(HPO:0007373) Degeneration of anterior horn cells(HPO:0002398) Abnormal upper motor neuron morphology(HPO:0002127) Degeneration of anterior horn cells(HPO:0002398) Abnormal peripheral nervous system morphology(HPO:0000759) Abnormal anterior horn cell morphology(HPO:0006802) Degeneration of anterior horn cells(HPO:0002398) MedDRA: |
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Database Frequency: | 14 / 7739 | ||||||||||||
Resource: |
All diseases associated with this symptom:
Amyotrophic lateral sclerosis | (Orphanet:803) |
Amyotrophic lateral sclerosis type 4 | (Orphanet:357043) |
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM | (OMIM:118301) |
Hereditary motor and sensory neuropathy, Okinawa type | (Orphanet:90117) |
Hereditary myoclonus - progressive distal muscular atrophy | (Orphanet:2590) |
MOTOR NEURON DISEASE WITH DEMENTIA AND OPHTHALMOPLEGIA | (OMIM:600333) |
PONTOCEREBELLAR HYPOPLASIA, TYPE 1A | (OMIM:607596) |
Pontocerebellar hypoplasia type 1 | (Orphanet:2254) |
Proximal spinal muscular atrophy type 2 | (Orphanet:83418) |
Proximal spinal muscular atrophy type 3 | (Orphanet:83419) |
Proximal spinal muscular atrophy type 4 | (Orphanet:83420) |
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 1 | (OMIM:604320) |
Spinal muscular atrophy with respiratory distress | (Orphanet:98920) |
X-linked distal arthrogryposis multiplex congenita | (Orphanet:1145) |