Qhov Kev Pabcuam Cov Neeg Tsis Txaus Siab (Genetically Handicapped Persons Program (GHPP)) suav nrog cov npe tshwj xeeb ntawm cov kab mob caj ces. Cov npe kab mob no tau teev tseg hauv California Txoj Cai Tswjfwm Ntiag Tug, Title 17.​​ 

GHPP Cov Kev Kho Mob Tsim Nyog Muaj xws li:​​ 

Cov Kab Mob Ntshav​​ 
Cystic Fibrosis​​ 
Kab mob ntawm lub paj hlwb thiab paj hlwb​​ 
Diseases of the Protein Metabolism​​ 
Kab mob ntawm Carbohydrates Metabolism​​ 
Kab mob ntawm Copper Metabolism​​ 
Von Hippel-Lindau Disease (VHL)​​  

Yog tias koj tus mob caj ces tsis nyob hauv cov npe saum toj no, koj tsis tsim nyog rau npe nrog GHPP. Thov hu rau GHPP rau cov lus nug ntawm 1-800-639-0597.​​  

Cov Kab Mob Ntshav​​ 

• Hemophilia lossis Factor Deficiency (FACTORS I, II, V, VII, VIII, IX, X, XI, XIII)​​ 
• Von Willebrand tus kab mob​​ 
• Congenital Hereditary Platelet Deficiency Diseases lossis kev ua haujlwm tsis zoo xws li Congenital Thrombasthenia (Glanzmann's Thrombasthenia) thiab Thrombocytopathia​​ 
• Hemoglobinopathies nrog Anemia:​​ 
• Sickle Cell Disease (Tsis yog mob kab mob)​​ 
• Thalassemia​​ 

Cystic Fibrosis (CF)​​ 

• Cystic Fibrosis (CF) (Tsis yog DHCS)​​ 

Kab mob ntawm lub paj hlwb thiab paj hlwb​​ 

• Huntington's Disease(HD)​​ 
• Joseph’s Disease(Spinocerebellar Ataxia III or SCA III)​​ 
  
• Friedrich’s Ataxia, ataxias due to spinocerebellar degeneration​​ 
• Hereditary Spastic Paraplegia​​ 
• Roussy-Levy Syndrome​​ 
• Refsum's Disease​​ 
• Charcot-Marie Tooth Syndrome (CMT Syndrome)​​ 

Cov kab mob ntawm Protein Metabolism​​ 

• Phenylketonuria (PKU)​​ 
• Tyrosinemia​​ 
• Kev cuam tshuam ntawm Metabolism ntawm Leucine, Isoleucine, Valine​​ 
• Hypervalinemia​​ 
• Intermittent Branched-Chain Ketonuria​​ 
• Leucine Induced / Leucinosis​​ 
• Maple Syrup Urine Disease (MSUD)​​ 
• Propionic Acidemia and Methylmalonic Acidemia​​ 
• Lactic thiab Pyruvate Metabolism Disorders​​ 
• Orotic keeb kwm (Pyrimidine Acidemia)​​ 
• Homocystinuria​​ 
• Hypermethioninemia​​ 
• Argininosuccinic Aciduria​​ 
• Citrullinemia​​ 
• Kev cuam tshuam ntawm Metabolism ntawm Ornithine, Citrulline, Argininosuccinic Acid, Arginine, thiab Ammonia​​ 
• Hyperammonemia​​ 
• Hyperornithinemia​​ 
  

Kab mob ntawm Carbohydrates Metabolism​​ 

• Galactosemia​​ 
• Galactose-1-Phosphate Uridyltransferase Deficiency​​ 
• Galactosuria​​  

Kab mob ntawm Copper Metabolism​​ 

• Wilson's Disease​​  

Von Hippel-Lindau Disease (VHL)​​