eRAM
encyclopedia of Rare Disease Annotation for Precision Medicine
| hyperemesis gravidarum | ||||
| Disease ID | 1169 |
|---|---|
| Disease | hyperemesis gravidarum |
| Definition | Intractable VOMITING that develops in early PREGNANCY and persists. This can lead to DEHYDRATION and WEIGHT LOSS. |
| Synonym | excess vomiting in pregnancy excessive pregnancy vomiting excessive vomiting in pregnancy excessive vomiting in pregnancy (disorder) excessive vomiting pregnancy gravidarum -hyperemesis gravidarum hyperemesis hyperemesis hyperemesis arising during pregnancy hyperemesis gravidarum [disease/finding] hyperemesis in pregnancy hyperemesis of pregnancy hyperemesis pregnancy pernicious vomiting of pregnancy persistent and/or vicious vomiting arising during pregnancy persistent or vicious vomiting arising during pregnancy pregnancy hyperemesis pregnancy pernicious vomiting vomiting, pernicious, of pregnancy |
| DOID | |
| UMLS | C0020450 |
| MeSH | |
| SNOMED-CT | |
| Comorbidity | UMLS | Disease | Sentences' Count(Total Sentences:20) C0043121 | wernicke's encephalopathy | 4 C0020550 | hyperthyroidism | 3 C0011570 | depression | 3 C0003467 | anxiety | 2 C0040156 | thyrotoxicosis | 2 C0235250 | hyperemesis | 2 C2267227 | bulimia nervosa | 1 C0007115 | thyroid cancer | 1 C0032046 | placenta previa | 1 C0040127 | thyroid crisis | 1 C0028754 | obesity | 1 C0006370 | bulimia | 1 C0043121 | wernicke encephalopathy | 1 C0007115 | thyroid ca | 1 C0024623 | gastric cancer | 1 C0002871 | anemia | 1 C0035078 | renal failure | 1 C0162429 | nutritional deficiency | 1 C0878544 | cardiomyopathy | 1 C0032827 | k deficiency | 1 |
| Curated Gene | (Waiting for update.) |
| Inferring Gene | (Waiting for update.) |
| Text Mined Gene | (Waiting for update.) |
| Locus | (Waiting for update.) |
| Disease ID | 1169 |
|---|---|
| Disease | hyperemesis gravidarum |
| Manually Symptom | UMLS | Name(Total Manually Symptoms:19) C2712335 | dehydration C2712332 | vomiting C2364072 | depression C2186532 | liver disease C1998045 | subclinical hyperthyroidism C1863307 | f syndrome C1420750 | wernicke-korsakoff syndrome C0850666 | helicobacter pylori infection C0281839 | esophageal rupture C0206083 | central pontine myelinolysis C0162275 | ketonuria C0043121 | wernicke's encephalopathy C0042880 | vitamin k deficiency C0027849 | neuroleptic malignant syndrome C0026848 | myopathy C0020550 | hyperthyroidism C0013473 | eating disorders C0008372 | intrahepatic cholestasis C0008370 | cholestasis |
| Text Mined Symptom | UMLS | Name | Sentences' Count(Total Symptoms:8) C0020550 | hyperthyroidism | 3 C0042963 | vomiting | 3 C0011175 | dehydration | 3 C0043121 | wernicke's encephalopathy | 3 C0011570 | depression | 3 C0042880 | vitamin k deficiency | 1 C0162275 | ketonuria | 1 C1998045 | subclinical hyperthyroidism | 1 |
Manually Genotype(Total Text Mining Genotypes:0) |
|---|
| (Waiting for update.) |
Text Mining Genotype(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
All Snps(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
GWASdb Annotation(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
GWASdb Snp Trait(Total Genotypes:0) | |
|---|---|
| (Waiting for update.) | |
Mapped by lexical matching(Total Items:0) |
|---|
| (Waiting for update.) |
Mapped by homologous gene(Total Items:0) |
|---|
| (Waiting for update.) |
| Disease ID | 1169 |
|---|---|
| Disease | hyperemesis gravidarum |
| Case | (Waiting for update.) |