Absent septum pellucidum

Symptom Information:

Symptom ID: HPO:0001331
Synonyms:
Absence of septum pellucidum [HPO:0001331]
Absence of the septum pellucidum [HPO:0001331]
Agenesis of the septum pellucidum [HPO:0001331]
Septum pellucidum agenesis [Orphanet:42630]
Absence of septum pellucidum (disorder) [Orphanet:42630]
Absence of septum pellucidum [Orphanet:42630]
Absence of septum pellucidum [OMIM:Absence of septum pellucidum]
Absence of the septum pellucidum [OMIM:Absence of the septum pellucidum]
Absent septum pellucidum [OMIM:Absent septum pellucidum]
Agenesis of the septum pellucidum [OMIM:Agenesis of the septum pellucidum]
Corpus callosum/septum pellucidum total/partial agenesis [Orphanet:42630]
Septum pellucidum agenesis [Orphanet:42630]
Septum pellucidum agenesis [MedDRA:10062267]
Quality:
Cross references:
Orphanet:42630 "Corpus callosum/septum pellucidum total/partial agenesis" [Orphanet:42630]
OMIM: "Absence of septum pellucidum" [OMIM:Absence of septum pellucidum]
OMIM: "Absence of the septum pellucidum" [OMIM:Absence of the septum pellucidum]
OMIM: "Absent septum pellucidum" [OMIM:Absent septum pellucidum]
OMIM: "Agenesis of the septum pellucidum" [OMIM:Agenesis of the septum pellucidum]
UMLS:C0431371 "Absence of septum pellucidum" [Orphanet:42630]
Is a (Direct Parents):
HPO         Abnormality of the septum pellucidum
Orphanet Structural anomalies of the nervous system
MedDRA Cerebral disorders congenital
Orphanet Agenesis of corpus callosum
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)
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)