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
- asymptomatic hyperammonemia
- MeSH ID
- No data
- Standard Disease Name
- asymptomatic hyperuricemia
- MeSH ID
- No data
- Standard Disease Name
- asymptomatic hypoglycaemia
- MeSH ID
- No data
- Standard Disease Name
- asymptomatic multiple myeloma
- MeSH ID
- No data
- Standard Disease Name
- asymptomatic periapical periodontitis
- MeSH ID
- No data
- Standard Disease Name
- ataxia
- MeSH ID
- No data
- Standard Disease Name
- ataxia and polyneuropathy, adult-onset
- MeSH ID
- No data
- Standard Disease Name
- ataxia and retinitis pigmentosa with isolated vitamin e deficiency
- MeSH ID
- No data
- Standard Disease Name
- ataxia neuropathy spectrum
- MeSH ID
- No data
- Standard Disease Name
- ataxia telangiectasia
- MeSH ID
- No data
- Standard Disease Name
- ataxia with lactic acidosis, type i
- MeSH ID
- No data
- Standard Disease Name
- ataxia with vitamin e deficiency
- MeSH ID
- No data
- Standard Disease Name
- ataxia, appendicular
- MeSH ID
- No data
- Standard Disease Name
- ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus
- MeSH ID
- No data
- Standard Disease Name
- ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia
- MeSH ID
- D004934
- Standard Disease Name
- ataxia, fatal x-linked, with deafness and loss of vision
- MeSH ID
- No data
- Standard Disease Name
- ataxia, friedreich-like, with isolated vitamin e deficiency
- MeSH ID
- No data
- Standard Disease Name
- ataxia, motor
- MeSH ID
- No data
- Standard Disease Name
- ataxia, sensory
- MeSH ID
- No data
- Standard Disease Name
- ataxia, sensory, 1, autosomal dominant
- MeSH ID
- No data
- Standard Disease Name
- ataxia, sensory, autosomal dominant
- MeSH ID
- No data
- Standard Disease Name
- ataxia, spastic, 1, autosomal dominant
- MeSH ID
- No data
- Standard Disease Name
- ataxia, spastic, 2, autosomal recessive (disorder)
- MeSH ID
- No data
- Standard Disease Name
- ataxia, spastic, 3, autosomal recessive
- MeSH ID
- No data
- Standard Disease Name
- ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation
- 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 |
|---|---|---|
| Asymptomatic hyperammonemia | asymptomatic hyperammonemia | No data |
| asymptomatic hyperuricemia | asymptomatic hyperuricemia | No data |
| Asymptomatic hypoglycaemia | asymptomatic hypoglycaemia | No data |
| Asymptomatic multiple myeloma | asymptomatic multiple myeloma | No data |
| Asymptomatic periapical periodontitis | asymptomatic periapical periodontitis | No data |
| Ataxia | ataxia | No data |
| Ataxia And Polyneuropathy, Adult-Onset | ataxia and polyneuropathy, adult-onset | No data |
| ATAXIA AND RETINITIS PIGMENTOSA WITH ISOLATED VITAMIN E DEFICIENCY | ataxia and retinitis pigmentosa with isolated vitamin e deficiency | No data |
| Ataxia Neuropathy Spectrum | ataxia neuropathy spectrum | No data |
| Ataxia Telangiectasia | ataxia telangiectasia | No data |
| Ataxia with Lactic Acidosis, Type I | ataxia with lactic acidosis, type i | No data |
| Ataxia with vitamin E deficiency | ataxia with vitamin e deficiency | No data |
| Ataxia, Appendicular | ataxia, appendicular | No data |
| ATAXIA, COMBINED CEREBELLAR AND PERIPHERAL, WITH HEARING LOSS AND DIABETES MELLITUS | ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus | No data |
| Ataxia, Early-Onset, With Oculomotor Apraxia And Hypoalbuminemia | ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia | D004934 |
| ATAXIA, FATAL X-LINKED, WITH DEAFNESS AND LOSS OF VISION | ataxia, fatal x-linked, with deafness and loss of vision | No data |
| ATAXIA, FRIEDREICH-LIKE, WITH ISOLATED VITAMIN E DEFICIENCY | ataxia, friedreich-like, with isolated vitamin e deficiency | No data |
| Ataxia, Motor | ataxia, motor | No data |
| Ataxia, Sensory | ataxia, sensory | No data |
| Ataxia, Sensory, 1, Autosomal Dominant | ataxia, sensory, 1, autosomal dominant | No data |
| Ataxia, Sensory, Autosomal Dominant | ataxia, sensory, autosomal dominant | No data |
| ATAXIA, SPASTIC, 1, AUTOSOMAL DOMINANT | ataxia, spastic, 1, autosomal dominant | No data |
| Ataxia, Spastic, 2, Autosomal Recessive (Disorder) | ataxia, spastic, 2, autosomal recessive (disorder) | No data |
| Ataxia, Spastic, 3, Autosomal Recessive | ataxia, spastic, 3, autosomal recessive | No data |
| ATAXIA, SPASTIC, CHILDHOOD-ONSET, AUTOSOMAL RECESSIVE, WITH OPTIC ATROPHY AND MENTAL RETARDATION | ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation | No data |