Abnormality of the corpus callosum

Symptom Information:

Symptom ID: HPO:0001273
Synonyms:
Abnormal corpus callosum [HPO:0001273]
Corpus callosum abnormality [HPO:0001273]
Abnormal corpus callosum [OMIM:Abnormal corpus callosum]
Corpus callosum abnormalities [OMIM:Corpus callosum abnormalities]
Corpus callosum abnormalities (in some patients) [OMIM:Corpus callosum abnormalities (in some patients)]
Quality:
Cross references:
OMIM: "Abnormal corpus callosum" [OMIM:Abnormal corpus callosum]
OMIM: "Corpus callosum abnormalities" [OMIM:Corpus callosum abnormalities]
OMIM: "Corpus callosum abnormalities (in some patients)" [OMIM:Corpus callosum abnormalities (in some patients)]
Is a (Direct Parents):
HPO         Abnormality of the cerebral white matter
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 20 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
5q14.3 microdeletion syndrome (Orphanet:228384)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Autosomal dominant spastic paraplegia type 4 (Orphanet:100985)
Autosomal recessive spastic ataxia with leukoencephalopathy (Orphanet:314603)
Autosomal recessive spastic paraplegia type 45 (Orphanet:320396)
Autosomal recessive spastic paraplegia type 7 (Orphanet:99013)
Bilateral generalized polymicrogyria (Orphanet:208447)
CEDNIK syndrome (Orphanet:66631)
Joubert syndrome 2 (OMIM:608091)
Lissencephaly due to LIS1 mutation (Orphanet:95232)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 14 (OMIM:614607)
MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS (OMIM:604317)
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency (Orphanet:1194)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Phenylketonuria (Orphanet:716)
Spastic paraplegia 63, autosomal recessive (OMIM:615686)
TARP syndrome (Orphanet:2886)
Temtamy syndrome (Orphanet:1777)
Wolf-Hirschhorn syndrome (Orphanet:280)