Single umbilical artery

Symptom Information:

Symptom ID: HPO:0001195
Synonyms:
Single umbilical artery (disorder) [Orphanet:34740]
Single umbilical artery [Orphanet:34740]
Single umbilical artery [OMIM:Single umbilical artery]
Single umbilical artery [MedDRA:10049807]
Quality:
Cross references:
Orphanet:34740 "Single umbilical artery" [Orphanet:34740]
OMIM: "Single umbilical artery" [OMIM:Single umbilical artery]
UMLS:C1384670 "Single umbilical artery" [Orphanet:34740]
Is a (Direct Parents):
HPO         Abnormal umbilical cord blood vessels
MedDRA Vascular malformations and acquired anomalies
HPO         Fetal ultrasound soft marker
HPO         Abnormality of the fetal cardiovascular system
Orphanet Structural anomalies of the cardio-circulatory system
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the cardiovascular system(HPO:0001626)
          Abnormality of the fetal cardiovascular system(HPO:0010948)
             Single umbilical artery(HPO:0001195)
       Abnormality of prenatal development or birth(HPO:0001197)
          Fetal ultrasound soft marker(HPO:0011425)
             Single umbilical artery(HPO:0001195)
          Abnormalities of placenta or umbilical cord(HPO:0001194)
             Abnormality of the umbilical cord(HPO:0010881)
                Abnormal umbilical cord blood vessels(HPO:0011403)
                   Single umbilical artery(HPO:0001195)
MedDRA:
Vascular disorders(MedDRA:10047065)
    Vascular disorders NEC(MedDRA:10047066)
       Vascular malformations and acquired anomalies(MedDRA:10047091)
          Single umbilical artery(HPO:0001195)
Database Frequency: 23 / 7739
Resource:

All diseases associated with this symptom:

19q13.11 microdeletion syndrome (Orphanet:217346)
3C syndrome (Orphanet:7)
Congenital alveolar capillary dysplasia (Orphanet:210122)
Congenital osteogenesis imperfecta - microcephaly - cataracts (Orphanet:2772)
Diabetic embryopathy (Orphanet:1926)
Emanuel syndrome (Orphanet:96170)
Familial caudal dysgenesis (Orphanet:1768)
Fibulo-ulnar hypoplasia - renal anomalies (Orphanet:2256)
Holzgreve-Wagner-Rehder syndrome (Orphanet:2167)
Lowry-MacLean syndrome (Orphanet:2409)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 17 (OMIM:615009)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 1 (OMIM:249000)
Mosaic trisomy 9 (Orphanet:99776)
Omphalocele syndrome, Shprintzen-Goldberg type (Orphanet:3164)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
Tetraamelia - multiple malformations (Orphanet:3301)
Ulbright-Hodes syndrome (Orphanet:3404)
Umbilical cord ulceration - intestinal atresia (Orphanet:3405)
VACTERL with hydrocephalus (Orphanet:3412)
VACTERL/VATER association (Orphanet:887)
Van den Ende-Gupta syndrome (Orphanet:2460)