Qhov Kev Pab Cuam Rau Cov Neeg Muaj Kev Tsis Taus Genetically Handicapped Persons (GHPP) muaj cov npe tshwj xeeb ntawm cov kab mob caj ces. Daim ntawv teev cov kab mob caj ces no tau teev tseg hauv California Code of Regulations, 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 koj tus mob caj ces tsis nyob hauv daim ntawv teev saum toj no, koj tsis tsim nyog rau npe nrog GHPP. Thov hu rau GHPP yog tias koj muaj 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​​ 

Mob Cystic Fibrosis (CF)​​ 

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

Kab mob ntawm lub paj hlwb thiab paj hlwb​​ 

• Huntington's Disease(HD)​​ 
• Kab mob Joseph (Spinocerebellar Ataxia III lossis SCA III)​​ 
  
• Friedrich's Ataxia, ataxias vim yog spinocerebellar degeneration​​ 
• Hereditary Spastic Paraplegia​​ 
• Roussy-Levy Syndrome​​ 
• Refsum's Disease​​ 
• Kab Mob Hniav Charcot-Marie (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​​ 
• Kab mob zis los ntawm kua txiv maple (MSUD)​​ 
• Propionic Acidemia thiab 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)​​