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Subjects (1-19 of 19)
Genetic Disorders
1

-- See Genetic Diseases, Inborn


Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero
2

-- See Also the narrower term Alpha 1-antitrypsin deficiency


3

-- See Also the narrower term Axenfeld-Rieger syndrome


4

-- See Also the narrower term Charcot-Marie-Tooth disease


5

-- See Also the narrower term Cystic fibrosis


6

-- See Also the narrower term Ehlers-Danlos syndrome


7

-- See Also the narrower term Epidermolysis bullosa


8

-- See Also the narrower term Fanconi's anemia


9

-- See Also the narrower term Friedreich's ataxia


10

-- See Also the narrower term Human chromosome abnormalities


11

-- See Also the narrower term Huntington's disease


12

-- See Also the narrower term Marfan syndrome


13

-- See Also Medical genetics



--subdivision Genetic aspects under individual diseases and types of diseases, e.g. Cancer--Genetic aspects; and subdivision Diseases--Genetic aspects under individual organs and regions of the body, e.g. Heart--Diseases--Genetic aspects
14

-- See Also the narrower term Metabolism, Inborn errors of


15

-- See Also the narrower term Mitochondrial DNA Abnormalities


16

-- See Also the narrower term Muscular dystrophy


17

-- See Also the narrower term Severe combined immunodeficiency


18

-- See Also the narrower term Velocardiofacial syndrome


19

-- See Also the narrower term Von Willebrand disease


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