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.
33,428 resultsSort: Disease Name descending
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- Standard Disease Name
- x-linked intellectual disability with cerebellar hypoplasia syndrome
- MeSH ID
- No data
- Standard Disease Name
- x-linked intellectual disability van esch type
- MeSH ID
- No data
- Standard Disease Name
- x-linked inherited disorder
- MeSH ID
- No data
- Standard Disease Name
- x-linked infantile spasms
- MeSH ID
- No data
- Standard Disease Name
- x-linked infantile spasm syndrome
- MeSH ID
- C538670
- Standard Disease Name
- x-linked infantile nystagmus
- MeSH ID
- No data
- Standard Disease Name
- x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia
- MeSH ID
- No data
- Standard Disease Name
- x-linked hypophosphatemia
- MeSH ID
- No data
- Standard Disease Name
- x-linked hypohidrotic ectodermal dysplasia
- MeSH ID
- D053358
- Standard Disease Name
- x-linked hypogammaglobulinemia
- MeSH ID
- No data
- Standard Disease Name
- x-linked hydrocephalus syndrome
- MeSH ID
- No data
- Standard Disease Name
- x-linked hereditary sensory and autonomic neuropathy with deafness
- MeSH ID
- No data
- Standard Disease Name
- x-linked hereditary motor and sensory neuropathy
- MeSH ID
- No data
- Standard Disease Name
- x-linked epilepsy-learning disabilities-behavior disorders syndrome
- MeSH ID
- No data
- Standard Disease Name
- x-linked emery-dreifuss muscular dystrophy
- MeSH ID
- No data
- Standard Disease Name
- x-linked dyskeratosis congenita
- MeSH ID
- D019871
- Standard Disease Name
- x-linked dyggve-melchior-clausen syndrome
- MeSH ID
- No data
- Standard Disease Name
- x-linked dominant inheritance
- MeSH ID
- No data
- Standard Disease Name
- x-linked dominant chondrodysplasia, chassaing-lacombe type
- MeSH ID
- No data
- Standard Disease Name
- x-linked dominant chondrodysplasia punctata
- MeSH ID
- No data
- Standard Disease Name
- x-linked csnb
- MeSH ID
- No data
- Standard Disease Name
- x-linked creatine transporter deficiency
- MeSH ID
- C535598
- Standard Disease Name
- x-linked complicated corpus callosum dysgenesis
- MeSH ID
- C564115
- Standard Disease Name
- x-linked combined immunodeficiency diseases
- MeSH ID
- No data
- Standard Disease Name
- x-linked cleft palate and ankyloglossia
- MeSH ID
- No data
| Disease NameCurrently sorted descending; click to toggle sort direction | Standard Disease NameClick to sort by this column | MeSH IDClick to sort by this column |
|---|---|---|
| X-linked intellectual disability with cerebellar hypoplasia syndrome | x-linked intellectual disability with cerebellar hypoplasia syndrome | No data |
| X-linked intellectual disability Van Esch type | x-linked intellectual disability van esch type | No data |
| X-Linked Inherited Disorder | x-linked inherited disorder | No data |
| X-Linked Infantile Spasms | x-linked infantile spasms | No data |
| X-Linked Infantile Spasm Syndrome | x-linked infantile spasm syndrome | C538670 |
| X-Linked Infantile Nystagmus | x-linked infantile nystagmus | No data |
| X-Linked Immunodeficiency With Magnesium Defect, Epstein-Barr Virus Infection And Neoplasia | x-linked immunodeficiency with magnesium defect, epstein-barr virus infection and neoplasia | No data |
| X-Linked Hypophosphatemia | x-linked hypophosphatemia | No data |
| X-Linked Hypohidrotic Ectodermal Dysplasia | x-linked hypohidrotic ectodermal dysplasia | D053358 |
| X-linked hypogammaglobulinemia | x-linked hypogammaglobulinemia | No data |
| X-Linked Hydrocephalus Syndrome | x-linked hydrocephalus syndrome | No data |
| X-Linked Hereditary Sensory And Autonomic Neuropathy With Deafness | x-linked hereditary sensory and autonomic neuropathy with deafness | No data |
| X-linked hereditary motor and sensory neuropathy | x-linked hereditary motor and sensory neuropathy | No data |
| X-Linked Epilepsy-Learning Disabilities-Behavior Disorders Syndrome | x-linked epilepsy-learning disabilities-behavior disorders syndrome | No data |
| X-Linked Emery-Dreifuss Muscular Dystrophy | x-linked emery-dreifuss muscular dystrophy | No data |
| X-Linked Dyskeratosis Congenita | x-linked dyskeratosis congenita | D019871 |
| X-Linked Dyggve-Melchior-Clausen Syndrome | x-linked dyggve-melchior-clausen syndrome | No data |
| X-linked dominant inheritance | x-linked dominant inheritance | No data |
| X-Linked Dominant Chondrodysplasia, Chassaing-Lacombe Type | x-linked dominant chondrodysplasia, chassaing-lacombe type | No data |
| X-Linked Dominant Chondrodysplasia Punctata | x-linked dominant chondrodysplasia punctata | No data |
| X-Linked Csnb | x-linked csnb | No data |
| X-Linked Creatine Transporter Deficiency | x-linked creatine transporter deficiency | C535598 |
| X-Linked Complicated Corpus Callosum Dysgenesis | x-linked complicated corpus callosum dysgenesis | C564115 |
| X-Linked Combined Immunodeficiency Diseases | x-linked combined immunodeficiency diseases | No data |
| X-Linked Cleft Palate And Ankyloglossia | x-linked cleft palate and ankyloglossia | No data |