Absent septum pellucidum
Symptom Information:
Symptom ID: | HPO:0001331 | |||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
MedDRA: Congenital, familial and genetic disorders(MedDRA:10010331) Neurological disorders congenital(MedDRA:10029299) Cerebral disorders congenital(MedDRA:10052634) Absent septum pellucidum(HPO:0001331) |
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Database Frequency: | 16 / 7739 | |||||||||||||
Resource: |
All diseases associated with this symptom:
1p36 deletion syndrome | (Orphanet:1606) |
Apert syndrome | (Orphanet:87) |
BRACHIAL AMELIA, CLEFT LIP, AND HOLOPROSENCEPHALY | (OMIM:601357) |
Craniotelencephalic dysplasia | (Orphanet:1528) |
FETAL AKINESIA DEFORMATION SEQUENCE | (OMIM:208150) |
Fetal akinesia deformation sequence | (Orphanet:994) |
HYDROLETHALUS SYNDROME 1 | (OMIM:236680) |
Hydrocephalus with stenosis of aqueduct of Sylvius | (Orphanet:2182) |
Hydrolethalus | (Orphanet:2189) |
MICROPHTHALMIA, SYNDROMIC 7 | (OMIM:309801) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Multiple congenital anomalies-hypotonia-seizures syndrome type 2 | (Orphanet:300496) |
Septo-optic dysplasia | (Orphanet:3157) |
TERATOCARCINOMA-DERIVED GROWTH FACTOR 1 | (OMIM:187395) |
Weaver syndrome | (Orphanet:3447) |
Wolf-Hirschhorn syndrome | (Orphanet:280) |