Loading disease data
| Disease | Prevalence | Drugs | Proteins | |
|---|---|---|---|---|
| Frontotemporal dementia 1 (FTD1) | Rare | 1 | 6 | |
| Parkinson-dementia syndrome (PARDE) | Uncommon | — | 6 | |
| Pick disease of the brain (PIDB) | Rare | 2 | 6 | |
| Progressive supranuclear palsy 1 (PSNP1) | Uncommon | — | 6 | |
| Amyotrophic lateral sclerosis (ALS) | Uncommon | 6 | 2 | |
| Frontotemporal dementia 2 (FTD2) | Rare | 11 | 2 | |
| Ischemic stroke (ISCHSTR) | N/A | 237 | 2 | |
| Schizophrenia (SCZD) | Uncommon | 277 | 2 | |
| Advanced sleep phase syndrome, familial, 2 (FASPS2) | N/A | — | 1 | |
| Al Kaissi syndrome (ALKAS) | N/A | — | 1 | |
| Alexander disease (ALXDRD) | Ultra-Rare | 2 | 1 | |
| Aminoacylase-1 deficiency (ACY1D) | Ultra-Rare | — | 1 | |
| Amyloidosis, hereditary systemic 3 (AMYLD3) | N/A | — | 1 | |
| Amyotrophic lateral sclerosis 12 with or without frontotemporal dementia (ALS12) | Uncommon | 6 | 1 | |
| Anencephaly 2 (ANPH2) | Very Rare | — | 1 | |
| Angelman syndrome (AS) | Uncommon | 10 | 1 | |
| Ataxia-telangiectasia-like disorder 2 (ATLD2) | Ultra-Rare | — | 1 | |
| Autism 19 (AUTS19) | Very Rare | 56 | 1 | |
| Carpal tunnel syndrome 1 (CTS1) | Uncommon | — | 1 | |
| Cerebral cavernous malformations 4 (CCM4) | Uncommon | — | 1 | |
| Cerebral cavernous malformations 5 (CCM5) | N/A | — | 1 | |
| Charcot-Marie-Tooth disease, axonal, type 2CC (CMT2CC) | N/A | — | 1 | |
| Charcot-Marie-Tooth disease, axonal, type 2D (CMT2D) | Ultra-Rare | — | 1 | |
| Charcot-Marie-Tooth disease, axonal, type 2F (CMT2F) | Ultra-Rare | — | 1 | |
| Charcot-Marie-Tooth disease, axonal, type 2L (CMT2L) | Ultra-Rare | — | 1 | |
| Charcot-Marie-Tooth disease, axonal, type 2N (CMT2N) | Ultra-Rare | — | 1 | |
| Charcot-Marie-Tooth disease, axonal, type 2V (CMT2V) | Ultra-Rare | — | 1 | |
| Charcot-Marie-Tooth disease, axonal, type 2Y (CMT2Y) | Ultra-Rare | — | 1 | |
| Charcot-Marie-Tooth disease, demyelinating, type 4D (CMT4D) | N/A | — | 1 | |
| Charcot-Marie-Tooth disease, X-linked dominant, 6 (CMTX6) | Ultra-Rare | — | 1 | |
| Coffin-Lowry syndrome (CLS) | Rare | — | 1 | |
| Cone dystrophy 3 (COD3) | Rare | — | 1 | |
| Congenital myopathy 4B, autosomal recessive (CMYO4B) | Ultra-Rare | — | 1 | |
| Cortical dysplasia, complex, with other brain malformations 6 (CDCBM6) | N/A | — | 1 | |
| Deafness, autosomal dominant, 74 (DFNA74) | N/A | — | 1 | |
| Deafness, autosomal dominant, 87 (DFNA87) | N/A | — | 1 | |
| Deafness, autosomal recessive, 116 (DFNB116) | N/A | — | 1 | |
| Deafness, autosomal recessive, 18A (DFNB18A) | N/A | — | 1 | |
| Deafness, autosomal recessive, 97 (DFNB97) | N/A | — | 1 | |
| Dementia, Lewy body (DLB) | Uncommon | 13 | 1 | |
| Developmental and epileptic encephalopathy 12 (DEE12) | Very Rare | — | 1 | |
| Developmental and epileptic encephalopathy 30 (DEE30) | Rare | 6 | 1 | |
| Developmental and epileptic encephalopathy 4 (DEE4) | Rare | — | 1 | |
| Developmental and epileptic encephalopathy 63 (DEE63) | Ultra-Rare | 6 | 1 | |
| Developmental and epileptic encephalopathy 87 (DEE87) | N/A | — | 1 | |
| Developmental and epileptic encephalopathy 89 (DEE89) | N/A | — | 1 | |
| Duchenne muscular dystrophy (DMD) | Rare | 54 | 1 | |
| Dystrophia myotonica 1 (DM1) | Common | 3 | 1 | |
| Encephalopathy, acute, infection-induced, 8, herpes-specific (IIAE8) | Very Rare | — | 1 | |
| Encephalopathy, familial, with neuroserpin inclusion bodies (FENIB) | Ultra-Rare | — | 1 |