Disease Code Coverage
- MeSH
- 13.1%
- OMIM
- 9.1%
- UMLS
- 19.2%
- ICD-10
- 6%
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Diseases
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- Standard Disease Name
- autosomal dominant tubulointerstitial kidney disease
- MeSH ID
- No data
- Standard Disease Name
- autosomal dominant vitreoretinochoroidopathy
- MeSH ID
- No data
- Standard Disease Name
- autosomal erythropoietic protoporphyria
- MeSH ID
- No data
- Standard Disease Name
- autosomal hemophilia a
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive agammaglobulinemia
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive ataxia, beauce type
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive centronuclear myopathy
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive cerebellar ataxia type 1
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive cerebellar ataxia with late-onset spasticity
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive cerebellar ataxia with oculomotor apraxia type 1
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to wwox deficiency
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive cerebelloparenchymal disorder type 3
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive cerebral atrophy
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive chorioretinopathy-microcephaly syndrome
- MeSH ID
- C565379
- Standard Disease Name
- autosomal recessive chronic granulomatous disease
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive congenital methemoglobinemia type i
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive cutis laxa type 1
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive cutis laxa type 2b
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive emery-dreifuss muscular dystrophy
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive facio-digito-genital syndrome
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive familial dystonia
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive fructose 1, 6-diphosphatase deficiency
- MeSH ID
- C537900
- Standard Disease Name
- autosomal recessive hereditary spastic paraplegia
- MeSH ID
- D015419
- Standard Disease Name
- autosomal recessive hyperimmunoglobulin m syndrome
- MeSH ID
- No data
- Standard Disease Name
- autosomal recessive hypohidrotic ectodermal dysplasia
- 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 dominant tubulointerstitial kidney disease | autosomal dominant tubulointerstitial kidney disease | No data |
| Autosomal Dominant Vitreoretinochoroidopathy | autosomal dominant vitreoretinochoroidopathy | No data |
| Autosomal Erythropoietic Protoporphyria | autosomal erythropoietic protoporphyria | No data |
| Autosomal Hemophilia A | autosomal hemophilia a | No data |
| Autosomal recessive agammaglobulinemia | autosomal recessive agammaglobulinemia | No data |
| Autosomal Recessive Ataxia, Beauce Type | autosomal recessive ataxia, beauce type | No data |
| Autosomal Recessive Centronuclear Myopathy | autosomal recessive centronuclear myopathy | No data |
| Autosomal Recessive Cerebellar Ataxia Type 1 | autosomal recessive cerebellar ataxia type 1 | No data |
| Autosomal Recessive Cerebellar Ataxia With Late-Onset Spasticity | autosomal recessive cerebellar ataxia with late-onset spasticity | No data |
| Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 | autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 | No data |
| Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WWOX deficiency | autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to wwox deficiency | No data |
| Autosomal Recessive Cerebelloparenchymal Disorder Type 3 | autosomal recessive cerebelloparenchymal disorder type 3 | No data |
| Autosomal Recessive Cerebral Atrophy | autosomal recessive cerebral atrophy | No data |
| Autosomal Recessive Chorioretinopathy-Microcephaly Syndrome | autosomal recessive chorioretinopathy-microcephaly syndrome | C565379 |
| Autosomal Recessive Chronic Granulomatous Disease | autosomal recessive chronic granulomatous disease | No data |
| Autosomal recessive congenital methemoglobinemia type I | autosomal recessive congenital methemoglobinemia type i | No data |
| Autosomal Recessive Cutis Laxa Type 1 | autosomal recessive cutis laxa type 1 | No data |
| Autosomal recessive cutis laxa type 2B | autosomal recessive cutis laxa type 2b | No data |
| Autosomal Recessive Emery-Dreifuss Muscular Dystrophy | autosomal recessive emery-dreifuss muscular dystrophy | No data |
| Autosomal Recessive Facio-Digito-Genital Syndrome | autosomal recessive facio-digito-genital syndrome | No data |
| Autosomal Recessive Familial Dystonia | autosomal recessive familial dystonia | No data |
| Autosomal Recessive Fructose 1, 6-Diphosphatase Deficiency | autosomal recessive fructose 1, 6-diphosphatase deficiency | C537900 |
| Autosomal Recessive Hereditary Spastic Paraplegia | autosomal recessive hereditary spastic paraplegia | D015419 |
| Autosomal recessive hyperimmunoglobulin M syndrome | autosomal recessive hyperimmunoglobulin m syndrome | No data |
| Autosomal Recessive Hypohidrotic Ectodermal Dysplasia | autosomal recessive hypohidrotic ectodermal dysplasia | No data |