Anencephaly

Symptom Information:

Symptom ID: HPO:0002323
Synonyms:
Anencephalus (disorder) [Orphanet:42060]
anencephaly [HPO:0002323]
Anencephaly [Orphanet:42060]
Anencephaly [OMIM:Anencephaly]
Anencephaly/acrania [Orphanet:42060]
Anencephaly [MedDRA:10002320]
Anencephalia [MedDRA:10002320]
Anencephalus [MedDRA:10002320]
Anencephalus and similar anomalies [MedDRA:10002320]
Anencephaly (1 patient) [OMIM:Anencephaly (1 patient)]
Acrania [Orphanet:42060]
Acrania (disorder) [Orphanet:42060]
Acraniate monster (disorder) [Orphanet:42060]
Quality:
Cross references:
Orphanet:42060 "Anencephaly/acrania" [Orphanet:42060]
OMIM: "Anencephaly" [OMIM:Anencephaly]
OMIM: "Anencephaly (1 patient)" [OMIM:Anencephaly (1 patient)]
UMLS:C2021655 "anencephaly" [HPO:0002323]
UMLS:C0002902 "Anencephaly" [Orphanet:42060]
UMLS:C0702169 "Acrania" [Orphanet:42060]
Is a (Direct Parents):
Orphanet Spinal dysraphism
MedDRA Cerebral disorders congenital
HPO         Aplasia/Hypoplasia of the cerebrum
Is a (Whole tree): HPO:
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Neurological disorders congenital(MedDRA:10029299)
       Cerebral disorders congenital(MedDRA:10052634)
          Anencephaly(HPO:0002323)
Database Frequency: 28 / 7739
Resource:

All diseases associated with this symptom:

Aminopterin/methotrexate embryofetopathy (Orphanet:1908)
Cantrell pentalogy (Orphanet:1335)
Craniorachischisis (Orphanet:63260)
Diabetic embryopathy (Orphanet:1926)
Diprosopia (Orphanet:1681)
Distal monosomy 13q (Orphanet:1590)
HYDROLETHALUS SYNDROME 1 (OMIM:236680)
HYDROLETHALUS SYNDROME 2 (OMIM:614120)
Hydrolethalus (Orphanet:2189)
Iniencephaly (Orphanet:63259)
Isolated anencephaly/exencephaly (Orphanet:1048)
Isolated spina bifida (Orphanet:823)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 1 (OMIM:249000)
Meckel syndrome, type 10 (OMIM:614175)
Meckel syndrome, type 2 (OMIM:603194)
Meckel syndrome, type 4 (OMIM:611134)
Meckel syndrome, type 5 (OMIM:611561)
Meckel syndrome, type 6 (OMIM:612284)
Medeira-Dennis-Donnai syndrome (Orphanet:2476)
NEURAL TUBE DEFECTS, SUSCEPTIBILITY TO (OMIM:182940)
NEURAL TUBE DEFECTS, X-LINKEDSPINA BIFIDA, X-LINKED, INCLUDED (OMIM:301410)
Neural tube closure defect (Orphanet:268357)
Schisis association (Orphanet:63862)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Trisomy 18 (Orphanet:3380)
VACTERL/VATER association (Orphanet:887)
XK aprosencephaly (Orphanet:3469)