Axonal loss
Symptom Information:
Symptom ID: | HPO:0003447 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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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) Abnormal peripheral nervous system morphology(HPO:0000759) Peripheral axonal degeneration(HPO:0000764) Axonal loss(HPO:0003447) MedDRA: |
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Database Frequency: | 11 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E | (Orphanet:93114) |
CEREBELLAR ATAXIA, BENIGN, WITH THERMOANALGESIA | (OMIM:212890) |
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM | (OMIM:118301) |
CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE | (OMIM:118230) |
Charcot-Marie-Tooth disease type 4D | (Orphanet:99950) |
Charcot-Marie-Tooth disease type 4J | (Orphanet:139515) |
Fatal mitochondrial disease due to combined oxidative phosphorylation deficiency 3 | (Orphanet:168566) |
Muscular dystrophy, Selcen type | (Orphanet:199340) |
Nasu-Hakola disease | (Orphanet:2770) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B | (Orphanet:308393) |