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 dominant juvenile parkinson disease
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant keratitis
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant larsen syndrome
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant late onset parkinson disease
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant lateral temporal lobe epilepsy
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant limb girdle muscular dystrophy type 1a
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant macrothrombocytopenia
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant myotubular myopathy
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant neovascular inflammatory vitreoretinopathy
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant neurohypophyseal diabetes insipidus
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant nocturnal frontal lobe epilepsy
- MeSH ID
- C579932
- Standard Disease Name
- autosomal dominant oculocutaneous albinism
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant omodysplasia
- MeSH ID
- C567664
- Standard Disease Name
- autosomal dominant optic atrophy plus syndrome
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant osteopetrosis
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant osteosclerosis, worth type
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant palmoplantar keratoderma and congenital alopecia
- MeSH ID
- C537050
- Standard Disease Name
- autosomal dominant parkinsonism
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant popliteal pterygium syndrome
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant primary hypomagnesemia with hypocalciuria
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant primary microcephaly
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant retinitis pigmentosa
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant spondylocostal dysostosis
- MeSH ID
- D014828
- Standard Disease Name
- autosomal dominant striatal neurodegeneration
- MeSH ID
- C563783
| 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 Dominant Juvenile Parkinson Disease | autosomal dominant juvenile parkinson disease | No data |
| Autosomal dominant keratitis | autosomal dominant keratitis | No data |
| Autosomal Dominant Larsen Syndrome | autosomal dominant larsen syndrome | No data |
| Autosomal dominant late onset Parkinson disease | autosomal dominant late onset parkinson disease | No data |
| Autosomal Dominant Lateral Temporal Lobe Epilepsy | autosomal dominant lateral temporal lobe epilepsy | No data |
| Autosomal dominant limb girdle muscular dystrophy type 1A | autosomal dominant limb girdle muscular dystrophy type 1a | No data |
| Autosomal Dominant Macrothrombocytopenia | autosomal dominant macrothrombocytopenia | No data |
| Autosomal Dominant Myopia-Midfacial Retrusion-Sensorineural Hearing Loss-Rhizomelic Dysplasia Syndrome | autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome | No data |
| Autosomal Dominant Myotubular Myopathy | autosomal dominant myotubular myopathy | No data |
| Autosomal dominant neovascular inflammatory vitreoretinopathy | autosomal dominant neovascular inflammatory vitreoretinopathy | No data |
| Autosomal Dominant Neurohypophyseal Diabetes Insipidus | autosomal dominant neurohypophyseal diabetes insipidus | No data |
| Autosomal Dominant Nocturnal Frontal Lobe Epilepsy | autosomal dominant nocturnal frontal lobe epilepsy | C579932 |
| Autosomal dominant oculocutaneous albinism | autosomal dominant oculocutaneous albinism | No data |
| Autosomal Dominant Omodysplasia | autosomal dominant omodysplasia | C567664 |
| Autosomal dominant optic atrophy plus syndrome | autosomal dominant optic atrophy plus syndrome | No data |
| Autosomal Dominant Osteopetrosis | autosomal dominant osteopetrosis | No data |
| Autosomal Dominant Osteosclerosis, Worth Type | autosomal dominant osteosclerosis, worth type | No data |
| Autosomal Dominant Palmoplantar Keratoderma And Congenital Alopecia | autosomal dominant palmoplantar keratoderma and congenital alopecia | C537050 |
| Autosomal Dominant Parkinsonism | autosomal dominant parkinsonism | No data |
| Autosomal Dominant Popliteal Pterygium Syndrome | autosomal dominant popliteal pterygium syndrome | No data |
| Autosomal dominant primary hypomagnesemia with hypocalciuria | autosomal dominant primary hypomagnesemia with hypocalciuria | No data |
| Autosomal Dominant Primary Microcephaly | autosomal dominant primary microcephaly | No data |
| Autosomal dominant retinitis pigmentosa | autosomal dominant retinitis pigmentosa | No data |
| Autosomal Dominant Spondylocostal Dysostosis | autosomal dominant spondylocostal dysostosis | D014828 |
| Autosomal Dominant Striatal Neurodegeneration | autosomal dominant striatal neurodegeneration | C563783 |