Intestinal malrotation

Symptom Information:

Symptom ID: HPO:0002566
Synonyms:
GUT MALROTATION [HPO:0002566]
Malrotation [HPO:0002566]
Congenital malrotation (morphologic abnormality) [Orphanet:26660]
Congenital malrotation of intestine (disorder) [Orphanet:26660]
Congenital malrotation of intestine [Orphanet:26660]
Gut malrotation [OMIM:Gut malrotation]
Intestinal malrotation [OMIM:Intestinal malrotation]
Malrotation [OMIM:Malrotation]
Intestinal/gut/bowel malrotation [Orphanet:26660]
Intestinal malrotation [Orphanet:26660]
Intestinal malrotation [MedDRA:10064024]
Mesenterium commune [MedDRA:10064024]
Intestinal malrotation (in some patients) [OMIM:Intestinal malrotation (in some patients)]
Intestinal malrotation (less common) [OMIM:Intestinal malrotation (less common)]
Intestinal malrotation (rare) [OMIM:Intestinal malrotation (rare)]
Intestinal malrotation (rare, in males) [OMIM:Intestinal malrotation (rare, in males)]
Stomach malrotation [Orphanet:26660]
Quality:
Cross references:
Orphanet:26660 "Intestinal/gut/bowel malrotation" [Orphanet:26660]
OMIM: "Gut malrotation" [OMIM:Gut malrotation]
OMIM: "Intestinal malrotation" [OMIM:Intestinal malrotation]
OMIM: "Malrotation" [OMIM:Malrotation]
OMIM: "Intestinal malrotation (in some patients)" [OMIM:Intestinal malrotation (in some patients)]
OMIM: "Intestinal malrotation (less common)" [OMIM:Intestinal malrotation (less common)]
OMIM: "Intestinal malrotation (rare)" [OMIM:Intestinal malrotation (rare)]
OMIM: "Intestinal malrotation (rare, in males)" [OMIM:Intestinal malrotation (rare, in males)]
UMLS:C0221210 "Congenital malrotation of intestine" [Orphanet:26660]
Is a (Direct Parents):
Orphanet Abnormality of the small intestine
HPO         Abnormality of the intestine
MedDRA Intestinal disorders congenital
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the gastrointestinal tract(HPO:0011024)
                Abnormality of the intestine(HPO:0002242)
                   Intestinal malrotation(HPO:0002566)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Gastrointestinal tract disorders congenital(MedDRA:10018018)
       Intestinal disorders congenital(MedDRA:10022646)
          Intestinal malrotation(HPO:0002566)
Database Frequency: 89 / 7739
Resource:

All diseases associated with this symptom:

12q14 microdeletion syndrome (Orphanet:94063)
1p36 deletion syndrome (Orphanet:1606)
1q44 microdeletion syndrome (Orphanet:238769)
22q11.2 deletion syndrome (Orphanet:567)
3C syndrome (Orphanet:7)
46,XX disorder of sex development - anorectal anomalies (Orphanet:2973)
Absent tibia - polydactyly - arachnoid cyst (Orphanet:3328)
Acroosteolysis, dominant type (Orphanet:955)
Auriculoocular anomalies - cleft lip (Orphanet:71270)
BOR syndrome (Orphanet:107)
Bladder exstrophy (Orphanet:93930)
Blepharophimosis-intellectual deficit syndrome due to UBE3B deficiency (Orphanet:329255)
Bohring-Opitz syndrome (Orphanet:97297)
COFFIN-SIRIS SYNDROME (OMIM:135900)
CONGENITAL SHORT BOWEL SYNDROME (OMIM:615237)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Cat-eye syndrome (Orphanet:195)
Cholestasis - pigmentary retinopathy - cleft palate (Orphanet:1415)
Chronic intestinal pseudo-obstruction (Orphanet:2978)
Cleft lip/palate - intestinal malrotation - cardiopathy (Orphanet:2001)
Cloacal exstrophy (Orphanet:93929)
Coffin-Siris syndrome (Orphanet:1465)
Congenital alveolar capillary dysplasia (Orphanet:210122)
Congenital contractural arachnodactyly (Orphanet:115)
Congenital short bowel syndrome (Orphanet:2301)
Congenital sodium diarrhea (Orphanet:103908)
Cornelia de Lange syndrome (Orphanet:199)
Curry-Jones syndrome (Orphanet:1553)
Desmosterolosis (Orphanet:35107)
Diabetic embryopathy (Orphanet:1926)
Diaphragmatic defect - limb deficiency - skull defect (Orphanet:2141)
Donnai-Barrow syndrome (Orphanet:2143)
Double uterus - hemivagina - renal agenesis (Orphanet:3411)
Ehlers-Danlos syndrome, musculocontractural type (Orphanet:2953)
Embryonary disorganization syndrome (Orphanet:1664)
Exstrophy-epispadias complex (Orphanet:322)
Familial intestinal malrotation - facial anomalies (Orphanet:2454)
Focal dermal hypoplasia (Orphanet:2092)
Fryns syndrome (Orphanet:2059)
Greenberg dysplasia (Orphanet:1426)
Growth delay - hydrocephaly - lung hypoplasia (Orphanet:3035)
HAJDU-CHENEY SYNDROME (OMIM:102500)
Holoprosencephaly - postaxial polydactyly (Orphanet:2166)
Hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome (Orphanet:293864)
INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED (OMIM:300048)
IVIC syndrome (Orphanet:2307)
Intellectual deficit, X-linked, Wittwer type (Orphanet:85291)
Jacobsen syndrome (Orphanet:2308)
KABUKI SYNDROME 1 (OMIM:147920)
Kabuki syndrome (Orphanet:2322)
Kapur-Toriello syndrome (Orphanet:2328)
Laryngo-tracheo-esophageal cleft - pulmonary hypoplasia (Orphanet:2005)
Lethal chondrodysplasia, Moerman type (Orphanet:1420)
Lethal multiple pterygium syndrome (Orphanet:33108)
Limb body wall complex (Orphanet:2369)
Lowry-MacLean syndrome (Orphanet:2409)
MITCHELL-RILEY SYNDROME (OMIM:615710)
MULTISYSTEMIC SMOOTH MUSCLE DYSFUNCTION SYNDROME (OMIM:613834)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 1 (OMIM:249000)
Meckel syndrome, type 2 (OMIM:603194)
Megacystis-microcolon-intestinal hypoperistalsis syndrome (Orphanet:2241)
Microgastria - limb reduction defect (Orphanet:2538)
Mosaic trisomy 9 (Orphanet:99776)
Multiple intestinal atresia (Orphanet:2300)
NPHP3-related Meckel-like syndrome (Orphanet:3032)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Oculofaciocardiodental syndrome (Orphanet:2712)
Okamoto syndrome (Orphanet:2729)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Pancreatic hypoplasia - diabetes - congenital heart disease (Orphanet:2255)
Pericardial and diaphragmatic defect (Orphanet:2847)
Pfeiffer syndrome type 2 (Orphanet:93259)
Pfeiffer syndrome type 3 (Orphanet:93260)
Prune belly syndrome (Orphanet:2970)
Renal-hepatic-pancreatic dysplasia (Orphanet:294415)
SHORT RIB-POLYDACTYLY SYNDROME, TYPE IIB (OMIM:615087)
Short rib-polydactyly syndrome (Orphanet:1505)
Short rib-polydactyly syndrome, Beemer-Langer type (Orphanet:93268)
Short rib-polydactyly syndrome, Majewski type (Orphanet:93269)
Short-rib thoracic dysplasia 3 with or without polydactyly (OMIM:613091)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Tetrasomy 12p (Orphanet:884)
Thoraco-abdominal enteric duplication (Orphanet:1759)
Thymic-renal-anal-lung dysplasia (Orphanet:3326)
Triploidy (Orphanet:3376)
VISCERAL NEUROPATHY, FAMILIAL, AUTOSOMAL RECESSIVE (OMIM:243180)
Wolfram syndrome 2 (OMIM:604928)