Anencephaly
Symptom Information:
Symptom ID: | HPO:0002323 | |||||||||||||
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) Anencephaly(HPO:0002323) |
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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) |