Intestinal malrotation
Symptom Information:
Symptom ID: | HPO:0002566 | |||||||||||||||||
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 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) |
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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) |