Cavum septum pellucidum

Symptom Information:

Symptom ID: HPO:0002389
Synonyms:
Large cavum septi pellucidi [HPO:0002389]
Persistent cavum septum pellucidum [HPO:0002389]
Widened cavum septum pellucidum [HPO:0002389]
Cavum septum pellucidum [OMIM:Cavum septum pellucidum]
Large cavum septi pellucidi [OMIM:Large cavum septi pellucidi]
Persistent cavum septum pellucidum [OMIM:Persistent cavum septum pellucidum]
Widened cavum septum pellucidum [OMIM:Widened cavum septum pellucidum]
Quality:
Cross references:
OMIM: "Cavum septum pellucidum" [OMIM:Cavum septum pellucidum]
OMIM: "Large cavum septi pellucidi" [OMIM:Large cavum septi pellucidi]
OMIM: "Persistent cavum septum pellucidum" [OMIM:Persistent cavum septum pellucidum]
OMIM: "Widened cavum septum pellucidum" [OMIM:Widened cavum septum pellucidum]
Is a (Direct Parents):
HPO         Abnormality of the septum pellucidum
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 13 / 7739
Resource:

All diseases associated with this symptom:

1p36 deletion syndrome (Orphanet:1606)
Aicardi syndrome (Orphanet:50)
Autosomal dominant Opitz G/BBB syndrome (Orphanet:306588)
FETAL AKINESIA DEFORMATION SEQUENCE (OMIM:208150)
Fetal akinesia deformation sequence (Orphanet:994)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17 (OMIM:615009)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Miller-Dieker syndrome (Orphanet:531)
Opitz G/BBB syndrome (Orphanet:2745)
SOTOS SYNDROME 1 (OMIM:117550)
Sotos syndrome (Orphanet:821)
Thrombocytopenia - absent radius (Orphanet:3320)
Wolf-Hirschhorn syndrome (Orphanet:280)