Breech presentation
Symptom Information:
Symptom ID: | HPO:0001623 | ||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of prenatal development or birth(HPO:0001197) Abnormal delivery(HPO:0001787) Breech presentation(HPO:0001623) MedDRA: Pregnancy, puerperium and perinatal conditions(MedDRA:10036585) Foetal complications(MedDRA:10016849) Foetal position and presentation abnormalities(MedDRA:10000190) Breech presentation(HPO:0001623) |
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Database Frequency: | 16 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
ARTHROGRYPOSIS, DISTAL, TYPE 2A | (OMIM:193700) |
Achondrogenesis type 1B | (Orphanet:93298) |
Arthrogryposis multiplex congenita | (Orphanet:1037) |
Ear-patella-short stature syndrome | (Orphanet:2554) |
Ehlers-Danlos syndrome type 7A | (Orphanet:99875) |
Ehlers-Danlos syndrome type 7B | (Orphanet:99876) |
Ehlers-Danlos syndrome, arthrochalasic type | (Orphanet:1899) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
Lethal Kniest-like dysplasia | (Orphanet:2347) |
MEIER-GORLIN SYNDROME 1 | (OMIM:224690) |
Meckel syndrome | (Orphanet:564) |
NEMALINE MYOPATHY 9 | (OMIM:615731) |
OSTEOGENESIS IMPERFECTA, TYPE VII | (OMIM:610682) |
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) | (OMIM:214100) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Zellweger syndrome | (Orphanet:912) |