Leukoencephalopathy

Symptom Information:

Symptom ID: HPO:0002352
Synonyms:
Leukoencephalopathy [OMIM:Leukoencephalopathy]
Leukoencephalopathy [MedDRA:10024382]
Quality:
Cross references:
OMIM: "Leukoencephalopathy" [OMIM:Leukoencephalopathy]
UMLS:C0270612 "Leukoencephalopathy" [HPO:0002352]
Is a (Direct Parents):
MedDRA Encephalopathies NEC
HPO         Abnormality of the cerebrum
Is a (Whole tree): HPO:
MedDRA:
Nervous system disorders(MedDRA:10029205)
    Encephalopathy(HPO:0001298)
       Encephalopathies NEC(MedDRA:10014632)
          Leukoencephalopathy(HPO:0002352)
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)