Disease Code Coverage
- MeSH
- 13.1%
- OMIM
- 9.1%
- UMLS
- 19.2%
- ICD-10
- 6%
Browse curated traditional medicine herb records with full-text search, relationship summaries, and distribution charts.
Showing 33,428 matching records.
Shows relationship scale by relation type for the current entity type.
| Disease NameCurrently sorted ascending; click to toggle sort direction | Standard Disease NameClick to sort by this column | MeSH IDClick to sort by this column |
|---|---|---|
| Akt2-Related Familial Partial Lipodystrophy | akt2-related familial partial lipodystrophy | No data |
| Al Awadi syndrome | al awadi syndrome | No data |
| AL KAISSI SYNDROME | al kaissi syndrome | No data |
| Al-Gazali-Bakalinova Syndrome | al-gazali-bakalinova syndrome | C564621 |
| Al-Raqad Syndrome | al-raqad syndrome | No data |
| Alacrima | alacrima | No data |
| Alacrima, Achalasia, And Mental Retardation Syndrome | alacrima, achalasia, and mental retardation syndrome | No data |
| ALACRIMA, CONGENITAL, AUTOSOMAL RECESSIVE | alacrima, congenital, autosomal recessive | No data |
| Alagille Syndrome | alagille syndrome | D007571 |
| Alagille Syndrome 1 | alagille syndrome 1 | No data |
| Alagille Syndrome 2 | alagille syndrome 2 | No data |
| Aland Island Eye Disease | aland island eye disease | No data |
| Alanine Aminotransferase Increased | alanine aminotransferase increased | No data |
| Alanine aminotransferase measurement | alanine aminotransferase measurement | No data |
| Alanine measurement | alanine measurement | No data |
| Alazami Syndrome | alazami syndrome | No data |
| ALAZAMI-YUAN SYNDROME | alazami-yuan syndrome | No data |
| Albers-Schonberg Disease, Autosomal Recessive | albers-schonberg disease, autosomal recessive | No data |
| Albers-Sch?Nberg Osteopetrosis | albers-sch?nberg osteopetrosis | D010022 |
| Albinism | albinism | No data |
| Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells | albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells | No data |
| Albinism, Ocular | albinism, ocular | D016117 |
| Albinism, Ocular, Type I | albinism, ocular, type i | No data |
| ALBINISM, OCULAR, WITH LATE-ONSET SENSORINEURAL DEAFNESS (disorder) | albinism, ocular, with late-onset sensorineural deafness (disorder) | No data |
| Albinism, Ocular, With Sensorineural Deafness | albinism, ocular, with sensorineural deafness | No data |