Vomiting

Symptom Information:

Symptom ID: HPO:0002013
Synonyms:
Emesis [HPO:0002013]
Vomiting (disorder) [Orphanet:27180]
Finding of vomiting (finding) [Orphanet:27180]
Vomiting symptom (finding) [Orphanet:27180]
Vomiting [Orphanet:27180]
Vomiting [OMIM:Vomiting]
Nausea/vomiting/regurgitation/merycism/hyperemesis [Orphanet:27180]
Vomiting [MedDRA:10047700]
Bilious vomiting [MedDRA:10047700]
Emesis [MedDRA:10047700]
Habit vomiting [MedDRA:10047700]
Hyperemesis [MedDRA:10047700]
Nausea and vomiting [MedDRA:10047700]
Nausea vomiting and diarrhea [MedDRA:10047700]
Nausea vomiting and diarrhoea [MedDRA:10047700]
Nausea with vomiting [MedDRA:10047700]
Persistent vomiting [MedDRA:10047700]
Vomited [MedDRA:10047700]
Vomiting alone [MedDRA:10047700]
Vomiting NOS [MedDRA:10047700]
Vomiting reflex [MedDRA:10047700]
Vomiting aggravated [MedDRA:10047700]
Vomiting of medication [MedDRA:10047700]
Tablet in vomitus [MedDRA:10047700]
Vomiting post chemotherapy [MedDRA:10047700]
Vomiting post radiotherapy [MedDRA:10047700]
Blennemesis [MedDRA:10047700]
Postprandial emesis [MedDRA:10047700]
Persistent vomiting [OMIM:Persistent vomiting]
Vomiting (HCP) [OMIM:Vomiting (HCP)]
Merycism [MedDRA:10027387]
Rumination (finding) [Orphanet:27180]
Rumination [Orphanet:27180]
Regurgitation [MedDRA:10067171]
Regurgitation (finding) [Orphanet:27180]
Regurgitates after swallowing (finding) [Orphanet:27180]
Regurgitation [Orphanet:27180]
Regurgitates after swallowing [Orphanet:27180]
Quality:
Cross references:
Orphanet:27180 "Nausea/vomiting/regurgitation/merycism/hyperemesis" [Orphanet:27180]
OMIM: "Vomiting" [OMIM:Vomiting]
OMIM: "Persistent vomiting" [OMIM:Persistent vomiting]
OMIM: "Vomiting (HCP)" [OMIM:Vomiting (HCP)]
UMLS:C0042963 "Vomiting" [HPO:0002013]
UMLS:C0042963 "Vomiting" [Orphanet:27180]
UMLS:C0232604 "Rumination" [Orphanet:27180]
UMLS:C2004489 "Regurgitation" [Orphanet:27180]
UMLS:C0232605 "Regurgitates after swallowing" [Orphanet:27180]
Is a (Direct Parents):
HPO         Nausea and vomiting
MedDRA Nausea and vomiting symptoms
Orphanet Functional anomalies of the digestive system
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)
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)