Vomiting
Symptom Information:
Symptom ID: | HPO:0002013 | ||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Quality: | |||||||||||||||||||||||||||||||||||||||
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) Abdominal symptom(HPO:0011458) Nausea and vomiting(HPO:0002017) Vomiting(HPO:0002013) MedDRA: Gastrointestinal disorders(MedDRA:10017947) Gastrointestinal signs and symptoms(MedDRA:10018012) Nausea and vomiting symptoms(MedDRA:10028817) Vomiting(HPO:0002013) |
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Database Frequency: | 191 / 7739 | ||||||||||||||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
3-@METHYLCROTONYL-CoA CARBOXYLASE 1 DEFICIENCY | (OMIM:210200) |
5-oxoprolinase deficiency | (Orphanet:33572) |
ALG11-CDG | (Orphanet:280071) |
ALG3-CDG | (Orphanet:79321) |
Acid phosphatase deficiency | (Orphanet:35121) |
Acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins | (Orphanet:217371) |
Acute intermittent porphyria | (Orphanet:79276) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Alpers syndrome | (Orphanet:726) |
Alström syndrome | (Orphanet:64) |
Amish infantile epilepsy syndrome | (Orphanet:171714) |
Argininemia | (Orphanet:90) |
Argininosuccinic aciduria | (Orphanet:23) |
Arterial calcification, generalized, of infancy, 1 | (OMIM:208000) |
Autosomal dominant spastic paraplegia type 29 | (Orphanet:101009) |
Autosomal dominant spastic paraplegia type 9 | (Orphanet:100990) |
Autosomal recessive distal renal tubular acidosis without deafness | (Orphanet:93609) |
Autosomal recessive infantile hypercalcemia | (Orphanet:300547) |
BARTTER SYNDROME, ANTENATAL, TYPE 1 | (OMIM:601678) |
BARTTER SYNDROME, ANTENATAL, TYPE 2 | (OMIM:241200) |
Bartter syndrome | (Orphanet:112) |
Biotinidase deficiency | (Orphanet:79241) |
Blue diaper syndrome | (Orphanet:94086) |
CARDIOFACIOCUTANEOUS SYNDROME 1 | (OMIM:115150) |
CELIAC DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:212750) |
CHARCOT-MARIE-TOOTH DISEASE WITH PTOSIS AND PARKINSONISM | (OMIM:118301) |
CHARCOT-MARIE-TOOTH DISEASE, GUADALAJARA NEURONAL TYPE | (OMIM:118230) |
CONGENITAL SHORT BOWEL SYNDROME | (OMIM:615237) |
CORTICOSTERONE METHYLOXIDASE TYPE I DEFICIENCY | (OMIM:203400) |
CYCLIC VOMITING SYNDROME | (OMIM:500007) |
CYSTINOSIS, NEPHROPATHIC | (OMIM:219800) |
Carbamoylphosphate synthetase deficiency | (Orphanet:147) |
Cardiofaciocutaneous syndrome | (Orphanet:1340) |
Carnitine palmitoyl transferase II deficiency, severe infantile form | (Orphanet:228305) |
Carnitine uptake deficiency | (Orphanet:158) |
Carnitine-acylcarnitine translocase deficiency | (Orphanet:159) |
Caroli disease | (Orphanet:53035) |
Carpenter-Waziri syndrome | (Orphanet:93973) |
Cholesteryl ester storage disease | (Orphanet:75234) |
Chronic intestinal pseudo-obstruction | (Orphanet:2978) |
Chudley-Lowry-Hoar syndrome | (Orphanet:93971) |
Chylomicron retention disease | (Orphanet:71) |
Citrullinemia type I | (Orphanet:247525) |
Classic galactosemia | (Orphanet:79239) |
Classic maple syrup urine disease | (Orphanet:268145) |
Classical phenylketonuria | (Orphanet:79254) |
Combined malonic and methylmalonic acidemia | (Orphanet:289504) |
Combined oxidative phosphorylation defect type 13 | (Orphanet:319514) |
Combined oxidative phosphorylation defect type 4 | (Orphanet:254925) |
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cells | (Orphanet:83620) |
Congenital short bowel syndrome | (Orphanet:2301) |
Cronkhite-Canada syndrome | (Orphanet:2930) |
Cystinosis | (Orphanet:213) |
Cytomegalic congenital adrenal hypoplasia | (Orphanet:95702) |
DIABETES INSIPIDUS, NEPHROGENIC, AUTOSOMAL | (OMIM:125800) |
DIABETES INSIPIDUS, NEPHROGENIC, X-LINKED | (OMIM:304800) |
DIARRHEA 7 | (OMIM:615863) |
EDEMA, FAMILIAL IDIOPATHIC, PREPUBERTAL | (OMIM:129840) |
ENTEROPATHY, FAMILIAL, WITH VILLOUS EDEMA AND IMMUNOGLOBULIN G2 DEFICIENCY | (OMIM:600351) |
ESOPHAGITIS, EOSINOPHILIC, 1 | (OMIM:610247) |
ESOPHAGITIS, EOSINOPHILIC, 2 | (OMIM:613412) |
Early-onset familial noncirrhotic portal hypertension | (ORPHA:494348) |
Eosinophilic esophagitis | (Orphanet:73247) |
Episodic ataxia type 3 | (Orphanet:79135) |
Fabry disease | (Orphanet:324) |
Familial dysautonomia | (Orphanet:1764) |
Familial hypoaldosteronism | (Orphanet:427) |
Familial lipoprotein lipase deficiency | (Orphanet:309015) |
Familial visceral myopathy | (Orphanet:2604) |
Galactose epimerase deficiency | (Orphanet:79238) |
Gaucher disease type 2 | (Orphanet:77260) |
Gaucher disease type 3 | (Orphanet:77261) |
Generalized congenital lipodystrophy with myopathy | (Orphanet:228429) |
Generalized pseudohypoaldosteronism type 1 | (Orphanet:171876) |
Glutaric acidemia type 3 | (Orphanet:35706) |
Glycogen storage disease due to acid maltase deficiency, late-onset | (Orphanet:420429) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type a | (Orphanet:79258) |
Glycogen storage disease due to glucose-6-phosphatase deficiency type b | (Orphanet:79259) |
HIRSCHSPRUNG DISEASE, SUSCEPTIBILITY TO, 1 | (OMIM:142623) |
HOMOZYGOUS 11p15-p14 DELETION SYNDROME | (OMIM:606528) |
HYPERPARATHYROIDISM, NEONATAL SELF-LIMITED PRIMARY, WITH HYPERCALCIURIA | (OMIM:239199) |
HYPERPHOSPHATEMIA, POLYURIA, AND SEIZURES | (OMIM:239350) |
HYPERTHERMIA, CUTANEOUS, WITH HEADACHES AND NAUSEA | (OMIM:145590) |
HYPOADRENOCORTICISM, FAMILIAL | (OMIM:240200) |
HYPOKALEMIC ALKALOSIS, FAMILIAL, WITH SPECIFIC RENAL TUBULOPATHY | (OMIM:241150) |
Hawkinsinuria | (Orphanet:2118) |
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 | (Orphanet:137681) |
Hereditary angioedema type 1 | (Orphanet:100050) |
Hereditary angioedema type 2 | (Orphanet:100051) |
Hereditary angioedema type 3 | (Orphanet:100054) |
Hereditary coproporphyria | (Orphanet:79273) |
Hereditary fructose intolerance | (Orphanet:469) |
Hirschsprung disease | (Orphanet:388) |
His bundle tachycardia | (Orphanet:3283) |
Holmes-Gang syndrome | (Orphanet:93970) |
Holocarboxylase synthetase deficiency | (Orphanet:79242) |
Hurler syndrome | (Orphanet:93473) |
Hyperammonemia due to N-acetylglutamate synthetase deficiency | (Orphanet:927) |
Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency | (Orphanet:401948) |
Hyperimmunoglobulinemia D with periodic fever | (Orphanet:343) |
Hyperinsulinism-hyperammonemia syndrome | (Orphanet:35878) |
Hyperlysinemia, type I | (OMIM:238700) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Hyperornithinemia-hyperammonemia-homocitrullinuria | (Orphanet:415) |
Hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome | (Orphanet:363694) |
Hypouricemia, renal, 1 | (OMIM:220150) |
Hypouricemia, renal, 2 | (OMIM:612076) |
INFLAMMATORY SKIN AND BOWEL DISEASE, NEONATAL, 2 | (OMIM:616069) |
INTESTINAL PSEUDOOBSTRUCTION, NEURONAL, CHRONIC IDIOPATHIC, X-LINKED | (OMIM:300048) |
Infantile hypophosphatasia | (Orphanet:247651) |
Intermittent maple syrup urine disease | (Orphanet:268173) |
Isobutyryl-CoA dehydrogenase deficiency | (Orphanet:79159) |
Isolated 3-methylcrotonyl-CoA carboxylase deficiency | (Orphanet:6) |
Isolated NADH-CoQ reductase deficiency | (Orphanet:2609) |
Isovaleric acidemia | (Orphanet:33) |
Juberg-Marsidi syndrome | (Orphanet:93972) |
KRABBE DISEASE | (OMIM:245200) |
Ketoacidosis due to beta-ketothiolase deficiency | (Orphanet:134) |
Krabbe disease | (Orphanet:487) |
LEIOMYOMATOSIS, DIFFUSE, WITH ALPORT SYNDROME | (OMIM:308940) |
LESCH-NYHAN SYNDROME | (OMIM:300322) |
Leigh syndrome with leukodystrophy | (Orphanet:255241) |
Lesch-Nyhan syndrome | (Orphanet:510) |
Lysinuric protein intolerance | (Orphanet:470) |
Lysosomal acid lipase deficiency | (Orphanet:275761) |
MEDIUM CHAIN 3-KETOACYL-CoA THIOLASE DEFICIENCY | (OMIM:602199) |
MELAS | (Orphanet:550) |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 1 | (OMIM:157300) |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 10 | (OMIM:610208) |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 11 | (OMIM:610209) |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 3 | (OMIM:607498) |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 5 | (OMIM:607508) |
MIGRAINE WITH OR WITHOUT AURA, SUSCEPTIBILITY TO, 6 | (OMIM:607516) |
MIGRAINE WITHOUT AURA, SUSCEPTIBILITY TO, 4 | (OMIM:607501) |
MIGRAINE, FAMILIAL TYPICAL, SUSCEPTIBILITY TO, 2 | (OMIM:300125) |
MITOCHONDRIAL DNA DEPLETION SYNDROME 1 (MNGIE TYPE) | (OMIM:603041) |
MPI-CDG | (Orphanet:79319) |
MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 2 | (OMIM:614299) |
Malonic aciduria | (Orphanet:943) |
Maternally-inherited Leigh syndrome | (Orphanet:255210) |
Medium chain acyl-CoA dehydrogenase deficiency | (Orphanet:42) |
Menkes disease | (Orphanet:565) |
Mevalonic aciduria | (Orphanet:29) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Mitochondrial encephalo-cardio-myopathy due to TMEM70 deficiency | (Orphanet:1194) |
Mitochondrial neurogastrointestinal encephalomyopathy | (Orphanet:298) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Multiple acyl-CoA dehydrogenase deficiency | (Orphanet:26791) |
Navajo neurohepatopathy | (Orphanet:255229) |
Neonatal hemochromatosis | (Orphanet:446) |
Nephrogenic diabetes insipidus | (Orphanet:223) |
Nephronophthisis 1 | (OMIM:256100) |
Niemann-Pick disease type A | (Orphanet:77292) |
Noonan syndrome-like disorder with loose anagen hair | (Orphanet:2701) |
Ornithine transcarbamylase deficiency | (Orphanet:664) |
PMM2-CDG | (Orphanet:79318) |
Pearson syndrome | (Orphanet:699) |
Pediatric systemic lupus erythematosus | (Orphanet:93552) |
Perinatal lethal hypophosphatasia | (Orphanet:247623) |
Polyarteritis nodosa, childhood-onset | (OMIM:615688) |
Porphyria due to ALA dehydratase deficiency | (Orphanet:100924) |
Porphyria variegata | (Orphanet:79473) |
Progeria - short stature - pigmented nevi | (Orphanet:2959) |
Propionic acidemia | (Orphanet:35) |
Proximal renal tubular acidosis | (Orphanet:47159) |
Proximal tubulopathy - diabetes mellitus - cerebellar ataxia | (Orphanet:3390) |
Psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency | (Orphanet:88618) |
Pyruvate dehydrogenase E3 deficiency | (Orphanet:2394) |
Renal pseudohypoaldosteronism type 1 | (Orphanet:171871) |
Renier-Gabreels-Jasper syndrome | (Orphanet:93975) |
Reticular dysgenesis | (Orphanet:33355) |
Short chain acyl-CoA dehydrogenase deficiency | (Orphanet:26792) |
Smith-Fineman-Myers syndrome | (Orphanet:93974) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Spinocerebellar ataxia type 25 | (Orphanet:101111) |
Succinyl-CoA:3-ketoacid CoA transferase deficiency | (Orphanet:832) |
Thiamine-responsive maple syrup urine disease | (Orphanet:268184) |
Transcobalamin deficiency | (Orphanet:859) |
VALINEMIA | (OMIM:277100) |
Very long chain acyl-CoA dehydrogenase deficiency | (Orphanet:26793) |
Vitamin B12-responsive methylmalonic acidemia | (Orphanet:28) |
Vitamin B12-responsive methylmalonic acidemia type cblA | (Orphanet:79310) |
Vitamin B12-responsive methylmalonic acidemia type cblB | (Orphanet:79311) |
Vitamin B12-unresponsive methylmalonic acidemia | (Orphanet:27) |
WOLMAN DISEASE WITH HYPOLIPOPROTEINEMIA AND ACANTHOCYTOSIS | (OMIM:278100) |
Wilson disease | (Orphanet:905) |
Wolman disease | (Orphanet:75233) |
X-linked creatine transporter deficiency | (Orphanet:52503) |
X-linked intellectual deficit - hypotonic face | (Orphanet:73220) |
X-linked spinocerebellar ataxia type 3 | (Orphanet:85297) |
[DEL] GLYCOGEN STORAGE DISEASE Ib | (OMIM:232220) |