The following pages link to SH3BP2
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Charcot–Marie–Tooth disease (links | edit)
- Joubert syndrome (links | edit)
- Wolff–Parkinson–White syndrome (links | edit)
- Cardiofaciocutaneous syndrome (links | edit)
- Tuberous sclerosis (links | edit)
- Noonan syndrome (links | edit)
- Li–Fraumeni syndrome (links | edit)
- Peutz–Jeghers syndrome (links | edit)
- Incontinentia pigmenti (links | edit)
- Signal transducing adaptor protein (links | edit)
- CADASIL (links | edit)
- 14-3-3 protein (links | edit)
- Coffin–Lowry syndrome (links | edit)
- Neurofibromatosis type I (links | edit)
- Bardet–Biedl syndrome (links | edit)
- Caveolin (links | edit)
- X-linked agammaglobulinemia (links | edit)
- SH2 domain (links | edit)
- Cowden syndrome (links | edit)
- Cherubism (links | edit)
- Neurofibromatosis type II (links | edit)
- Carpenter syndrome (links | edit)
- Metachondromatosis (links | edit)
- McCune–Albright syndrome (links | edit)
- Costello syndrome (links | edit)
- GRB7 (links | edit)
- ZAP70 deficiency (links | edit)
- Carney complex (links | edit)
- Bannayan–Riley–Ruvalcaba syndrome (links | edit)
- Pleckstrin homology domain (links | edit)
- Seckel syndrome (links | edit)
- Pseudohypoaldosteronism (links | edit)
- SMAD (protein) (links | edit)
- Pseudopseudohypoparathyroidism (links | edit)
- GRB2 (links | edit)
- Noonan syndrome with multiple lentigines (links | edit)
- MYD88 (links | edit)
- TNF receptor associated factor (links | edit)
- Hypohidrotic ectodermal dysplasia (links | edit)
- Cortactin (links | edit)
- Paxillin (links | edit)
- Death-inducing signaling complex (links | edit)
- Aarskog–Scott syndrome (links | edit)
- Myotonic dystrophy (links | edit)
- Polycystic liver disease (links | edit)
- Juvenile primary lateral sclerosis (links | edit)
- Oguchi disease (links | edit)
- Rab escort protein 1 (links | edit)
- TRAF6 (links | edit)
- IRF3 (links | edit)