Disease Code Coverage
- MeSH
- 13.1%
- OMIM
- 9.1%
- UMLS
- 19.2%
- ICD-10
- 6%
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Diseases
Browse curated traditional medicine herb records with full-text search, relationship summaries, and distribution charts.
Showing 33,428 matching records.
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- Standard Disease Name
- apolipoprotein a-i (baltimore) phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein a-i (giessen) phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein a-i (marburg) phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein a-i (milano) phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein a-i (munster3b) phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein a-i (munster3c) phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein a-i (munster4) phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein a-i (norway) phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein a-i deficiency
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein a-iv polymorphism, apoa4*1/apoa4*2 phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein b assay
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein c-ii (auckland) phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein c-ii (bari) phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein c-ii (padova) phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein c-ii (paris) phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein c-ii (san francisco)
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein c-ii (wakayama) phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein c-ii deficiency
- MeSH ID
- D008072
- Standard Disease Name
- apolipoprotein c-ii deficiency (disorder)
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein c-ii variant phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein c-iii deficiency
- MeSH ID
- No data
- Standard Disease Name
- apolipoprotein c-iii, nonglycosylated phenotype
- MeSH ID
- No data
- Standard Disease Name
- apolipoproteins e measurement (procedure)
- MeSH ID
- No data
- Standard Disease Name
- apoptotic dna damage
- MeSH ID
- No data
- Standard Disease Name
- apparent mineralocorticoid excess
- MeSH ID
- No data
| Disease NameCurrently sorted ascending; click to toggle sort direction | Standard Disease NameClick to sort by this column | MeSH IDClick to sort by this column |
|---|---|---|
| APOLIPOPROTEIN A-I (BALTIMORE) PHENOTYPE | apolipoprotein a-i (baltimore) phenotype | No data |
| APOLIPOPROTEIN A-I (GIESSEN) PHENOTYPE | apolipoprotein a-i (giessen) phenotype | No data |
| APOLIPOPROTEIN A-I (MARBURG) PHENOTYPE | apolipoprotein a-i (marburg) phenotype | No data |
| APOLIPOPROTEIN A-I (MILANO) PHENOTYPE | apolipoprotein a-i (milano) phenotype | No data |
| APOLIPOPROTEIN A-I (MUNSTER3B) PHENOTYPE | apolipoprotein a-i (munster3b) phenotype | No data |
| APOLIPOPROTEIN A-I (MUNSTER3C) PHENOTYPE | apolipoprotein a-i (munster3c) phenotype | No data |
| APOLIPOPROTEIN A-I (MUNSTER4) PHENOTYPE | apolipoprotein a-i (munster4) phenotype | No data |
| APOLIPOPROTEIN A-I (NORWAY) PHENOTYPE | apolipoprotein a-i (norway) phenotype | No data |
| Apolipoprotein A-I Deficiency | apolipoprotein a-i deficiency | No data |
| APOLIPOPROTEIN A-IV POLYMORPHISM, APOA4*1/APOA4*2 PHENOTYPE | apolipoprotein a-iv polymorphism, apoa4*1/apoa4*2 phenotype | No data |
| Apolipoprotein B Assay | apolipoprotein b assay | No data |
| APOLIPOPROTEIN C-II (AUCKLAND) PHENOTYPE | apolipoprotein c-ii (auckland) phenotype | No data |
| APOLIPOPROTEIN C-II (BARI) PHENOTYPE | apolipoprotein c-ii (bari) phenotype | No data |
| APOLIPOPROTEIN C-II (PADOVA) PHENOTYPE | apolipoprotein c-ii (padova) phenotype | No data |
| APOLIPOPROTEIN C-II (PARIS) PHENOTYPE | apolipoprotein c-ii (paris) phenotype | No data |
| APOLIPOPROTEIN C-II (SAN FRANCISCO) | apolipoprotein c-ii (san francisco) | No data |
| apolipoprotein C-II (Wakayama) phenotype | apolipoprotein c-ii (wakayama) phenotype | No data |
| Apolipoprotein C-Ii Deficiency | apolipoprotein c-ii deficiency | D008072 |
| Apolipoprotein C-II Deficiency (disorder) | apolipoprotein c-ii deficiency (disorder) | No data |
| APOLIPOPROTEIN C-II VARIANT PHENOTYPE | apolipoprotein c-ii variant phenotype | No data |
| Apolipoprotein C-III Deficiency | apolipoprotein c-iii deficiency | No data |
| APOLIPOPROTEIN C-III, NONGLYCOSYLATED PHENOTYPE | apolipoprotein c-iii, nonglycosylated phenotype | No data |
| Apolipoproteins E measurement (procedure) | apolipoproteins e measurement (procedure) | No data |
| Apoptotic DNA damage | apoptotic dna damage | No data |
| Apparent mineralocorticoid excess | apparent mineralocorticoid excess | No data |