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
- autosomal aneuploidy
- MeSH ID
- No data
- Standard Disease Name
- autosomal chromosome disorders
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant beta2-microglobulinic amyloidosis
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant brachyolmia
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant cerebellar ataxia
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant charcot-marie-tooth disease type 2 due to kif5a mutation
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant charcot-marie-tooth disease type 2d
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant charcot-marie-tooth disease type 2f
- MeSH ID
- C535413
- Standard Disease Name
- autosomal dominant charcot-marie-tooth disease type 2y
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant compelling helio ophthalmic outburst syndrome
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant congenital benign spinal muscular atrophy
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant contiguous gene syndrome
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant cutis laxa
- MeSH ID
- C562627
- Standard Disease Name
- autosomal dominant emery-dreifuss muscular dystrophy (disorder)
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant familial dystonia
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant focal segmental glomerulosclerosis
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant hereditary pancreatitis
- MeSH ID
- C537262
- Standard Disease Name
- autosomal dominant hyper-ige syndrome
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant hyperinsulinism due to kir6.2 deficiency
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant hyperinsulinism due to sur1 deficiency
- MeSH ID
- D001859
- Standard Disease Name
- autosomal dominant hypocalcemia
- MeSH ID
- C535992
- Standard Disease Name
- autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder)
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant hypophosphatemic rickets
- MeSH ID
- D001778
- Standard Disease Name
- autosomal dominant ichthyosis
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant intermediate charcot-marie-tooth disease with neuropathic pain
- 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 |
|---|---|---|
| Autosomal aneuploidy | autosomal aneuploidy | No data |
| Autosomal Chromosome Disorders | autosomal chromosome disorders | No data |
| Autosomal dominant beta2-microglobulinic amyloidosis | autosomal dominant beta2-microglobulinic amyloidosis | No data |
| Autosomal Dominant Brachyolmia | autosomal dominant brachyolmia | No data |
| Autosomal dominant cerebellar ataxia | autosomal dominant cerebellar ataxia | No data |
| Autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation | autosomal dominant charcot-marie-tooth disease type 2 due to kif5a mutation | No data |
| Autosomal dominant Charcot-Marie-Tooth disease type 2D | autosomal dominant charcot-marie-tooth disease type 2d | No data |
| Autosomal Dominant Charcot-Marie-Tooth Disease Type 2F | autosomal dominant charcot-marie-tooth disease type 2f | C535413 |
| Autosomal Dominant Charcot-Marie-Tooth Disease Type 2Y | autosomal dominant charcot-marie-tooth disease type 2y | No data |
| Autosomal dominant compelling helio ophthalmic outburst syndrome | autosomal dominant compelling helio ophthalmic outburst syndrome | No data |
| Autosomal Dominant Congenital Benign Spinal Muscular Atrophy | autosomal dominant congenital benign spinal muscular atrophy | No data |
| Autosomal dominant contiguous gene syndrome | autosomal dominant contiguous gene syndrome | No data |
| Autosomal Dominant Cutis Laxa | autosomal dominant cutis laxa | C562627 |
| Autosomal Dominant Emery-Dreifuss Muscular Dystrophy (Disorder) | autosomal dominant emery-dreifuss muscular dystrophy (disorder) | No data |
| Autosomal Dominant Familial Dystonia | autosomal dominant familial dystonia | No data |
| Autosomal dominant focal segmental glomerulosclerosis | autosomal dominant focal segmental glomerulosclerosis | No data |
| Autosomal Dominant Hereditary Pancreatitis | autosomal dominant hereditary pancreatitis | C537262 |
| Autosomal Dominant Hyper-Ige Syndrome | autosomal dominant hyper-ige syndrome | No data |
| Autosomal dominant hyperinsulinism due to Kir6.2 deficiency | autosomal dominant hyperinsulinism due to kir6.2 deficiency | No data |
| Autosomal dominant hyperinsulinism due to SUR1 deficiency | autosomal dominant hyperinsulinism due to sur1 deficiency | D001859 |
| Autosomal dominant hypocalcemia | autosomal dominant hypocalcemia | C535992 |
| Autosomal Dominant Hypohidrotic Ectodermal Dysplasia Syndrome (Disorder) | autosomal dominant hypohidrotic ectodermal dysplasia syndrome (disorder) | No data |
| Autosomal dominant hypophosphatemic rickets | autosomal dominant hypophosphatemic rickets | D001778 |
| Autosomal dominant ichthyosis | autosomal dominant ichthyosis | No data |
| Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain | autosomal dominant intermediate charcot-marie-tooth disease with neuropathic pain | No data |