Patent urachus

Patent urachus is a type of congenital urachal anomaly (see this term) characterized by a persistent communication between the bladder and the umbilicus, secondary to non occlusion of the urachal lumen, manifesting as clear drainage from the umbilicus.



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Total: 51 (papers)

   


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)		 PMID
(PMCID)
5
(4.0%)		 1620482
 [Persistent multiple urachal complex. Echographic-surgical correlations].
Bergami GL, Inserra A, Ciprandi G, Barbuti D, Di Mario M, Boglino C.
Minerva Chir. 1992;47(9):879-83.
Ovarian cyst
Homo sapiens Male Ultrasonography Urachus
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 26

HPO ID Term # of case reports
HP:0030754 Allantoic cyst 7
HP:0000969 Edema 4
HP:0025615 Abscess 3
HP:0030654 Umbilical cord cyst 2
HP:0000021 Megacystis 1
HP:0000047 Hypospadias 1
HP:0000048 Bifid scrotum 1
HP:0000076 Vesicoureteral reflux 1
HP:0000126 Hydronephrosis 1
HP:0000252 Microcephaly 1
HP:0000347 Micrognathia 1
HP:0000506 Telecanthus 1
HP:0000581 Blepharophimosis 1
HP:0000796 Urethral obstruction 1
HP:0001195 Single umbilical artery 1
HP:0001369 Arthritis 1
HP:0001537 Umbilical hernia 1
HP:0001847 Long hallux 1
HP:0002014 Diarrhea 1
HP:0002664 Neoplasm 1
HP:0002982 Tibial bowing 1
HP:0004383 Hypoplastic left heart 1
HP:0012620 Cloacal abnormality 1
HP:0030868 Monorchism 1
HP:0031274 Hypovolemic shock 1
HP:0100548 Exstrophy 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID