DNA mutations are the only way evolution can make changes in life for evolution to be true.
Yet, there are no genetic mutations ever found that make a life better for a species.
There is however an enormous number of mutations that makes life worse.
This is a list of only some of the diseases caused by genetic disorders, and this list is only
humans. |
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Aceruloplasminemia
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Achondrogenesis type II
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Achondroplasia
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Acute intermittent porphyria
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Adenylosuccinate lyase deficiency
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Adrenoleukodystrophy
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ALA dehydratase deficiency
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Alexander disease
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Alkaptonuria
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Alpha-1 antitrypsin deficiency
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Alstrom syndrome
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Alzheimer disease
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Amelogenesis Imperfecta
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Amyotrophic lateral sclerosis
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Androgen insensitivity syndrome
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Anemia
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Angelman syndrome
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Apert syndrome
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Ataxia-telangiectasia
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Beare-Stevenson
cutis gyrata syndrome
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Benjamin syndrome
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Beta thalassemia
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Biotinidase deficiency
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Bladder cancer
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Bloom syndrome
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Bone diseases
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Breast cancer
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Birt-Hogg-Dubé syndrome
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CADASIL
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CGD Chronic
Granulomatous Disorder
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Camptomelic dysplasia
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Canavan disease
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Cancer
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Celiac Disease
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Charcot-Marie-Tooth disease
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Cockayne syndrome
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Coffin-Lowry syndrome
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Collagenopathy, types II and XI
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Colorectal Cancer
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Congenital erythropoietic porphyria
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Congenital heart disease
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Congenital hypothyroidism
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Connective tissue disease
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Cowden syndrome
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Cri du chat
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Crohn’s disease, fibrostenosing
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Crouzon syndrome
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Crouzonodermoskeletal syndrome
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Degenerative
nerve diseases
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Developmental disabilities
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DiGeorge syndrome
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Distal
spinal muscular atrophy, type V
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Down syndrome
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Dwarfism
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Ehlers-Danlos syndrome
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Erythropoietic protoporphyria
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Fabry disease
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Facial
injuries and disorders
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factor V Leiden thrombophilia
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Familial adenomatous polyposis
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Familial dysautonomia
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FG syndrome
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Fragile X syndrome
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Friedreich’s ataxia
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G6PD deficiency
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Galactosemia
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Gaucher disease
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Genetic brain disorders
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Harlequin Ichthyosis
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Head and
brain malformations
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Hearing
disorders and deafness
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Hearing
problems in children
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Hemochromatosis
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Hemophilia
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Hepatoerythropoietic porphyria
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Hereditary coproporphyria
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Hereditary Multiple Exostoses
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Hereditary nonpolyposis colorectal
cancer
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Homocystinuria
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Huntington’s disease
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Hyperoxaluria, primary
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Hyperphenylalaninemia
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Hypochondrogenesis
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Hypochondroplasia
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Incontinentia Pigmenti
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Infantile-onset
ascending hereditary spastic paralysis
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Infertility
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Jackson-Weiss syndrome
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Joubert syndrome
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Klinefelter syndrome
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Kniest dysplasia
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Krabbe disease
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Lesch-Nyhan syndrome
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Leukodystrophies
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Li-Fraumeni syndrome
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Lipoprotein lipase deficiency,
familial
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Male genital disorders
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Marfan syndrome
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McCune-Albright syndrome
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McLeod syndrome
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Mediterranean fever, familial
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Menkes syndrome
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Metabolic disorders
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Methemoglobinemia#beta-globin type
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Methylmalonic acidemia
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Micro syndrome
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Microcephaly
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Movement disorders
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Mowat-Wilson syndrome
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Mucopolysaccharidosis (MPS I)
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Muenke syndrome
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Muscular dystrophy
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Muscular dystrophy, Duchenne and
Becker type
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Myotonic dystrophy
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Neurofibromatosis type I
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Neurofibromatosis type II
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Neurologic diseases
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Neuromuscular disorders
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Nonsyndromic deafness
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Noonan syndrome
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Osteogenesis imperfecta
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Otospondylomegaepiphyseal dysplasia
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Pantothenate
kinase-associated neurodegeneration
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Patau Syndrome (Trisomy 13)
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Pendred syndrome
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Peutz-Jeghers syndrome
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Pfeiffer syndrome
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Phenylketonuria
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Porphyria
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Prader-Willi syndrome
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Primary pulmonary hypertension
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Prion disease
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Propionic acidemia
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Protein C deficiency
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Protein S deficiency
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Pseudo-Gaucher disease
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Pseudoxanthoma elasticum
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Retinal disorders
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Retinoblastoma
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Rett syndrome
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Rubinstein-Taybi syndrome
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Severe achondroplasia with developmental delay and acanthosis nigrans
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Sickle cell anemia
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Skin
pigmentation disorders
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Smith Lemli Opitz Syndrome
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Speech and
communication disorders
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Spinal-bulbar
muscular atrophy
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Spinal muscular atrophy
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Spinocerebellar ataxia
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Spondyloepimetaphyseal
dysplasia, Strudwick type
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Spondyloepiphyseal dysplasia
congenita
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Stickler syndrome
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Tay-Sachs disease
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Tetrahydrobiopterin deficiency
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Thanatophoric dysplasia
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Thiamine-responsive
megaloblastic anemia with diabetes mellitus and sensorineural deafness
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Thyroid disease
Tourette’s Syndrome
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Treacher Collins syndrome
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Triple X syndrome
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Tuberous sclerosis
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Turner syndrome
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Usher syndrome
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Variegate porphyria
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Von Hippel-Lindau disease
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Waardenburg syndrome
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Weissenbacher-Zweymüller syndrome
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Wilson disease
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Wolf-Hirschhorn syndrome
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Xeroderma Pigmentosum
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X-linked severe combined immunodeficiency
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