| Descriptor English: | Cloacal Exstrophy |
| Descriptor Spanish: | Extrofia Cloacal |
| Descriptor Portuguese: | Extrofia Cloacal |
| Descriptor French: | Without translation |
| Entry term(s): |
Cloacal Exstrophies Congenital Vesico intestinal Fissure Congenital Vesico-intestinal Fissure Congenital Vesico-intestinal Fissures Congenital Vesicointestinal Fissure Congenital Vesicointestinal Fissures Exstrophies, Cloacal Exstrophy, Cloacal Fissure, Congenital Vesico-intestinal Fissure, Congenital Vesicointestinal Fissures, Congenital Vesico-intestinal Fissures, Congenital Vesicointestinal Vesico-intestinal Fissure, Congenital Vesico-intestinal Fissures, Congenital Vesicointestinal Fissure, Congenital Vesicointestinal Fissures, Congenital |
| Tree number(s): |
C06.198.050.500 C12.050.351.875.132.500 C12.050.351.968.829.132.500 C12.200.706.132.500 C12.200.777.829.132.500 C12.800.132.500 C12.950.829.132.500 C16.131.314.094.500 C16.131.939.132.500 |
| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D000099005 |
| Scope note: | A rare congenital malformation that affects the development of the urinary, digestive, and REPRODUCTIVE SYSTEMS due to CLOACA malformations. In this condition, the large intestine develops outside the abdominal cavity, with the bladder connected to it. Due to this abnormal connection between the colon and the bladder, urine and stool can mix, and there is often no anus. |
| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
| Previous Indexing: |
Bladder Exstrophy(1972-2024) |
| Public MeSH Note: | 2025 |
| History Note: | 2025 |
| DeCS ID: | 60934 |
| Unique ID: | D000099005 |
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents |
| Date Established: | 2025/01/01 |
| Date of Entry: | 2024/08/09 |
| Revision Date: | 2024/05/22 |
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Cloacal Exstrophy
- Preferred
Congenital Vesicointestinal Fissure
- Related but not broader or narrower
| Concept UI |
M000767746 |
| Scope note | A rare congenital malformation that affects the development of the urinary, digestive, and REPRODUCTIVE SYSTEMS due to CLOACA malformations. In this condition, the large intestine develops outside the abdominal cavity, with the bladder connected to it. Due to this abnormal connection between the colon and the bladder, urine and stool can mix, and there is often no anus. |
| Preferred term | Cloacal Exstrophy |
| Entry term(s) |
Cloacal Exstrophies Exstrophies, Cloacal Exstrophy, Cloacal |
| Concept UI |
M000767747 |
| Preferred term | Congenital Vesicointestinal Fissure |
| Entry term(s) |
Congenital Vesico intestinal Fissure Congenital Vesico-intestinal Fissure Congenital Vesico-intestinal Fissures Congenital Vesicointestinal Fissures Fissure, Congenital Vesico-intestinal Fissure, Congenital Vesicointestinal Fissures, Congenital Vesico-intestinal Fissures, Congenital Vesicointestinal Vesico-intestinal Fissure, Congenital Vesico-intestinal Fissures, Congenital Vesicointestinal Fissure, Congenital Vesicointestinal Fissures, Congenital |
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