Peripheral demyelination
Symptom Information:
| Symptom ID: | HPO:0011096 | ||||||
| Synonyms: |
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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 peripheral myelination(HPO:0003130) Peripheral demyelination(HPO:0011096) MedDRA: Nervous system disorders(MedDRA:10029205) Demyelinating disorders(MedDRA:10012303) Demyelinating disorders NEC(MedDRA:10012302) Peripheral demyelination(HPO:0011096) |
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| Database Frequency: | 28 / 7739 | ||||||
| Resource: |
All diseases associated with this symptom:
| Abetalipoproteinemia | (Orphanet:14) |
| Autosomal dominant Charcot-Marie-Tooth disease type 2J | (Orphanet:99943) |
| Autosomal dominant slowed nerve conduction velocity | (Orphanet:140481) |
| Autosomal recessive intermediate Charcot-Marie-Tooth disease type A | (Orphanet:217055) |
| Brain demyelination due to methionine adenosyltransferase deficiency | (Orphanet:168598) |
| Charcot-Marie-Tooth disease type 1B | (Orphanet:101082) |
| Charcot-Marie-Tooth disease type 4F | (Orphanet:99952) |
| Charcot-Marie-Tooth disease type 4H | (Orphanet:99954) |
| Congenital cataracts - facial dysmorphism - neuropathy | (Orphanet:48431) |
| Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
| Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
| KRABBE DISEASE | (OMIM:245200) |
| Krabbe disease | (Orphanet:487) |
| Leber plus disease | (Orphanet:99718) |
| Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency | (Orphanet:5) |
| METACHROMATIC LEUKODYSTROPHY | (OMIM:250100) |
| METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY | (OMIM:249900) |
| Multiple sulfatase deficiency | (Orphanet:585) |
| NEUROPATHY, WITH PARAPROTEIN IN SERUM, CEREBROSPINAL FLUID AND URINE | (OMIM:162600) |
| Nasu-Hakola disease | (Orphanet:2770) |
| Neurologic Waardenburg-Shah syndrome | (Orphanet:163746) |
| OPTIC ATROPHY WITH DEMYELINATING DISEASE OF CNS | (OMIM:165200) |
| OPTIC ATROPHY, HEARING LOSS, AND PERIPHERAL NEUROPATHY, AUTOSOMALRECESSIVE | (OMIM:258650) |
| Peripheral motor neuropathy - dysautonomia | (Orphanet:2400) |
| Recessive mitochondrial ataxia syndrome | (Orphanet:94125) |
| Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A | (Orphanet:308386) |
| Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B | (Orphanet:308393) |
| Tangier disease | (Orphanet:31150) |