Cavum septum pellucidum
Symptom Information:
Symptom ID: | HPO:0002389 | |||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 13 / 7739 | |||||||
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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) |