http://www.ncbi.nlm.nih.gov/genome/guide/HsChr11.shtml
and a neurodegenerative syndrome. Some diseases associated with chromosome 11 mutations Ataxia_telangiectasia Beckwith-wiedemann_syndrome Bardet-biedl_syndrome 1 LONG_QT_SYNDROME 1 Wilms Tumor Type
http://www.ncbi.nlm.nih.gov/genome/guide/HsChr21.shtml
for Human Chr. 21 Chromosome 21 Disease Genes Some diseases associated with chromosome 21 mutations Holoprosencephaly 1 Trisomy_21 (Down_syndrome) Usher Syndrome,
http://www.ncbi.nlm.nih.gov/genome/guide/HsChr4.shtml
Some diseases associated with chromosome 4 mutations Huntington_disease Juvenile Periodontitis Wolf-Hirschhorn Syndrome Wolfram_syndrome See OMIM or Genes
http://www.ncbi.nlm.nih.gov/disease/Transporters.html
syndrome Polycystic_kidney_disease Sickle_cell anemia Wilson's disease Zellweger_syndrome TRANSPORTERS, CHANNELS AND PUMPS that reside in cell_membranes are key to maintaining the right balance
http://www.ncbi.nlm.nih.gov/genome/guide/HsChr3.shtml
Cornelia De_lange_syndrome von Hippel-Lindau Syndrome Acute_myeloid_leukemia See OMIM or Genes and Disease for additional examples and detailed information.
http://www.ncbi.nlm.nih.gov/genome/guide/HsChr2.shtml
for Human Chr. 2 Chromosome 2 Disease Genes Some diseases associated with chromosome 2 mutations Alstrom Syndrome Holoprosencephaly 2 Tibial Muscular_dystrophy Autosomal Recessive Deafness
http://www.ncbi.nlm.nih.gov/disease/Muscle.html
Muscle and bone Duchenne muscular_dystrophy Ellis-van_creveld_syndrome Marfan_syndrome Myotonic_dystrophy Spinal muscular_atrophy THE SKELETON provides an anchor point against
While the gene for Ellis-van_creveld_syndrome has_been_mapped,
http://www.ncbi.nlm.nih.gov/disease/Signals.html
Signals Ataxia_telangiectasia Baldness Cockayne_syndrome Glaucoma SRY:
ataxia_telangiectasia and Cockayne_syndrome. Faulty DNA repair mechanisms are_invoked also in pathogenesis,
http://www.ncbi.nlm.nih.gov/genome/guide/HsChr20.shtml
National Cancer Institute Some diseases associated with chromosome 20 mutations Alagille_syndrome Corneal Dystrophy, polymorphous SCID,
http://www.ncbi.nlm.nih.gov/genome/guide/HsChr15.shtml
for Human Chr. 15 Chromosome 15 Disease Genes Prader-willi_syndrome is_caused by a deletion of a specific portion of the chromosome 15 inherited from the paternal lineage. Some diseases associated with chromosome 15 mutations
Amytrophic Lateral Sclerosis 5 Bloom_syndrome Prader-willi_syndrome Tay-sachs_disease See OMIM or Genes and Disease for additional examples and detailed information. OMIM
http://www.ncbi.nlm.nih.gov/genome/guide/HsChr9.shtml
Type C Nail-patella_syndrome See OMIM
http://www.ncbi.nlm.nih.gov/genome/guide/HsChr18.shtml
2 Stanford 279 RH 3 Genethon 136 Link 4 Disease Genes Some diseases associated with chromosome 18 mutations Colorectal Cancer Holoprosencephaly 4 Niemann-pick_disease,
http://www.ncbi.nlm.nih.gov/disease/Brain.html
The nervous_system Alzheimer_disease Amyotrophic_lateral_sclerosis Angelman_syndrome Charcot-marie-tooth_disease Epilepsy Essential_tremor Fragile_x_syndrome Friedreich's ataxia Huntington_disease Niemann-pick_disease
Parkinson_disease Prader-willi_syndrome Rett_syndrome Spinocerebellar atrophy Williams_syndrome THE BRAIN and nervous_system form an intricate network of electrical signals that are responsible_for coordinating muscles, the senses, speech,