Abnormality of the periventricular white matter

Symptom Information:

Symptom ID: HPO:0002518
Synonyms:
PERIVENTRICULAR WHITE MATTER ABNORMALITIES [HPO:0002518]
Periventricular white matter abnormalities [OMIM:Periventricular white matter abnormalities]
Periventricular white matter abnormalities (in some patients) [OMIM:Periventricular white matter abnormalities (in some patients)]
White matter abnormalities, periventricular [OMIM:White matter abnormalities, periventricular]
Quality:
Cross references:
OMIM: "Periventricular white matter abnormalities" [OMIM:Periventricular white matter abnormalities]
OMIM: "Periventricular white matter abnormalities (in some patients)" [OMIM:Periventricular white matter abnormalities (in some patients)]
OMIM: "White matter abnormalities, periventricular" [OMIM:White matter abnormalities, periventricular]
Is a (Direct Parents):
HPO         Leukoencephalopathy
HPO         Punctate periventricular T2 hyperintense foci
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 24 / 7739
Resource:

All diseases associated with this symptom:

5q14.3 microdeletion syndrome (Orphanet:228384)
Adult polyglucosan body disease (Orphanet:206583)
Autosomal recessive spastic paraplegia type 11 (Orphanet:2822)
Autosomal recessive spastic paraplegia type 35 (Orphanet:171629)
Autosomal recessive spastic paraplegia type 54 (Orphanet:320380)
Cerebroretinal vasculopathy (Orphanet:3421)
Cerebrotendinous xanthomatosis (Orphanet:909)
Christianson syndrome (Orphanet:85278)
Encephalopathy due to prosaposin deficiency (Orphanet:139406)
HERNS syndrome (Orphanet:63261)
Hereditary vascular retinopathy (Orphanet:71291)
MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY (OMIM:606369)
METACHROMATIC LEUKODYSTROPHY DUE TO SAPOSIN B DEFICIENCY (OMIM:249900)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 2 (OMIM:613156)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH MENTAL RETARDATION),TYPE B, 6 (OMIM:608840)
Monosomy 22q13 (Orphanet:48652)
Multiple sulfatase deficiency (Orphanet:585)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2A (OMIM:277470)
PONTOCEREBELLAR HYPOPLASIA, TYPE 2D (OMIM:613811)
PORETTI-BOLTSHAUSER SYNDROME (OMIM:615960)
Pontocerebellar hypoplasia type 2 (Orphanet:2524)
Retinal vasculopathy and cerebral leukodystrophy (Orphanet:247691)
SPASTIC PARAPLEGIA 47, AUTOSOMAL RECESSIVE (OMIM:614066)
Spastic paraplegia 63, autosomal recessive (OMIM:615686)