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cirrhosis
- ... in each cell and a more severe, cystic fibrosis-causing mutation in the other copy of the ... gene have been identified in people with cystic fibrosis. Most of these mutations change single protein building ...
- ... gene have been identified in people with congenital fibrosis of the extraocular muscles (CFEOM). These mutations cause ... This Health Condition CFEOM CFEOM1 DKFZp779C159 FEOM FEOM1 Fibrosis of extraocular muscles, congenital, 1, autosomal dominant fibrosis ...
- ... cancer and a progressive lung disease called pulmonary fibrosis. Many affected individuals also develop a serious condition ... people with the progressive lung disease idiopathic pulmonary fibrosis. This condition causes scar tissue (fibrosis) to build ...
- ... About This Health Condition Some people with cystic fibrosis-like syndrome have a mutation or a normal ... polymorphism) in the SCNN1B gene. People with cystic fibrosis-like syndrome (also known as atypical cystic fibrosis ...
- ... cancer and a progressive lung disease called pulmonary fibrosis. Many affected individuals also develop a serious condition ... people with the progressive lung disease idiopathic pulmonary fibrosis. This condition causes scar tissue (fibrosis) to build ...
- ... About This Health Condition Some people with cystic fibrosis-like syndrome have a mutation or a normal ... polymorphism) in the SCNN1A gene. People with cystic fibrosis-like syndrome (also known as atypical cystic fibrosis ...
- ... About This Health Condition Some people with cystic fibrosis-like syndrome have a mutation or a normal ... polymorphism) in the SCNN1G gene. People with cystic fibrosis-like syndrome (also known as atypical cystic fibrosis ...
- ... been found to cause North American Indian childhood cirrhosis, a chronic liver disease identified in a First ... About This Health Condition CIR1A_HUMAN CIRH1A cirhin cirrhosis, autosomal recessive 1A (cirhin) FLJ14728 FLJ17146 KIAA1988 NAIC ...
- ... mutations in the PHOX2A gene can cause congenital fibrosis of the extraocular muscles (CFEOM). These mutations are ... Amero K, Engle EC. Neurological features of congenital fibrosis of the extraocular muscles type 2 with mutations ...
- ... in people with hypermanganesemia with dystonia, polycythemia, and cirrhosis (HMDPC, also known as hypermanganesemia with dystonia 1). ... polycythemia); and liver abnormalities, including irreversible liver disease (cirrhosis).Mutations in the SLC30A10 gene impair the transport ...
