Leukoencephalopathy
Symptom Information:
Symptom ID: | HPO:0002352 | ||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: Nervous system disorders(MedDRA:10029205) Encephalopathy(HPO:0001298) Encephalopathies NEC(MedDRA:10014632) Leukoencephalopathy(HPO:0002352) |
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Database Frequency: | 32 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
3-methylglutaconic aciduria type 1 | (Orphanet:67046) |
AICARDI-GOUTIERES SYNDROME 1 | (OMIM:225750) |
Adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | (Orphanet:313808) |
Autosomal dominant familial hematuria - retinal arteriolar tortuosity - contractures | (Orphanet:73229) |
Autosomal recessive spastic ataxia with leukoencephalopathy | (Orphanet:314603) |
CACH syndrome | (Orphanet:135) |
CADASIL | (Orphanet:136) |
CLN4A disease | (Orphanet:228340) |
Coats plus syndrome | (Orphanet:313838) |
Congenital lactic acidosis, Saguenay-Lac-St. Jean type | (Orphanet:70472) |
Cystic leukoencephalopathy without megalencephaly | (Orphanet:85136) |
Hypomyelination with brain stem and spinal cord involvement and leg spasticity | (Orphanet:363412) |
Hypotonia with lactic acidemia and hyperammonemia | (Orphanet:137908) |
Isolated succinate-CoQ reductase deficiency | (Orphanet:3208) |
L-2-hydroxyglutaric aciduria | (Orphanet:79314) |
LEUKOENCEPHALOPATHY WITH ATAXIA | (OMIM:615651) |
LEUKOENCEPHALOPATHY, ARTHRITIS, COLITIS, AND HYPOGAMMAGLOBULINEMA | (OMIM:608809) |
LEUKOENCEPHALOPATHY, BRAIN CALCIFICATIONS, AND CYSTS | (OMIM:614561) |
Leukoencephalopathy - dystonia - motor neuropathy | (Orphanet:163684) |
Leukoencephalopathy - metaphyseal chondrodysplasia | (Orphanet:83629) |
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate | (Orphanet:314051) |
Leukoencephalopathy with brain stem and spinal cord involvement - lactate elevation | (Orphanet:137898) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) | (OMIM:603041) |
MUSCULAR DYSTROPHY, ADULT-ONSET, WITH LEUKOENCEPHALOPATHY | (OMIM:253590) |
Mitochondrial neurogastrointestinal encephalomyopathy | (Orphanet:298) |
Nasu-Hakola disease | (Orphanet:2770) |
PORENCEPHALY 1 | (OMIM:175780) |
Pontocerebellar hypoplasia, type 9 | (OMIM:615809) |
Porencephaly | (Orphanet:2940) |
Ribose 5-phosphate isomerase deficiency | (OMIM:608611) |
Severe combined immunodeficiency due to adenosine deaminase deficiency | (Orphanet:277) |