Here I present: Victor McKusick, “Mendelian Inheritance in Man”, 1966, Chromosome 19. This book was printed in twelve (12) editions from 1966 to 1998, shown ABOVE. Ninety-eight (98) traits of chromosome #19 are listed BELOW.
Region 19p1 Traits.
Fucosyltransferase-6 deficiency.
Hypocalciuric hypercalcemia, type II.
Leukemia, myeloid/lymphoid or mixed-lineage.
Wegener granulomatosis autoantigen.
Persistent Müllerian duct syndrome, type I.
Diabetes mellitus, insulin-resistant.
Leukemia, T-cell acute lymphobloid.
Mycobacterial and salmonella infections, susceptibility to.
Hemiplegic migraine, familial.
Ataxia, spinocerebellar and cerebellar.
Mannosidosis, alpha, types I and II.
Alzeheimer disease, late onset.
Glomerulosclerosis, focal segmental.
Hypercalcemia, familial benign, Oklahoma type, type III.
Charcot-Leyden crystal protein.
Malignant hyperthermia susceptibility.
Osteodysplasia, polycystic lipomembranous.
Maple syrup urine disease, type 1a.
Heart block, progressive familial, type.
3-methylglutaconiacaciduria, type III.
Meconium ileus in cystic fibrosis, susceptibility to.
Retinitis pigmentosa, late-onset dominant.
Diabetes mellitus, noninsulin-dependent.
Hyperferritinemia cataract syndrome.
Hypogonadism, hypergonadotropic.
Retinitis pigmentosa, autosomal dominant.
Ectodactyl, ectodermal dysplasia, cleft lip/palate.
Ataxia, cerebellar, Cayman type.
Convulsions, familial febrile.
Region 19q1 Traits.
Guanidinoacetate methyltransferase deficiency.
Leukemia, acute lymphoblastic.
Atherosclerosis, susceptibility to.
Malaria, cerebral, susceptibility.
Thyroid carcinoma, nonmedullary.
Low density lipoprotein receptor.
Hypercholesterolemia, familial.
Epiphyseal dysplasia, multiple.
Severe-combined, immunodeficiency disease.
Benign familial infantile convulsions.
Spondylocostal dysostosis, autosomal recessive.
Spastic paraplegia, autosomal dominant.
Nephrosis, congenital, Finnish type.
Generalized epilepsy with febrile seizures plus.
Microcephaly, autosomal recessive.
Hyperlipoproteinemia, types 1b and III.
Myocardial infarction susceptibility.
Cytochrome P450 (coumarin resistance).
Nicotine addiction, protection from.
Xeroderma pigmentosum, group D.
Herpes virus entry mediator B.
Leukemia, T-cell acute lymphoblastic.
Cardiomyopathy, familial hypertrophic.
Here I presented: Victor McKusick, “Mendelian Inheritance in Man”, 1966, Chromosome 19. Ninety-eight (98) traits of chromosome #19 were listed ABOVE.
HUMAN BODY COMPOSITION.
WATER 60%.
PROTEIN 16%
FAT 16%.
MINERAL 6%.
CARBOHYDRATE 1%.
NUCLEIC ACID 1%.
The “Table of Consanguinity” of bloodline names of familial relationships is shown BELOW. Mendelian Inheritance is a pair of genes of a Person (one gene from each Parent). This means that a generation pattern of the gene is observed in the “Table of Consanguinity”.
