Hypertension, essential, susceptibility to.
Schizophrenia, neurophysiologic, defect in.
Spherocytosis, hereditary, Japanese type.
Amyotrophic lateral sclerosis, juvenile recessive.
Dyserythropoietic anemia, congenital, type III.
Deafness, autosomal recessive.
Leukemia, acute promyelocytic, PML/RARA type.
Cardiomyopathy, familial hypertrophic.
Epilepsy, nocturnal frontal lobe, type 2.
Diabetes mellitus, insulin-dependent.
Prader-Willi/Angelman syndrome (paternally imprinted).
Human coronavirus sensitivity.
Albinism, oculocutaneous, type II and ocular.
Cardiomyopathy, dilated and familial hypertrophic.
Microcephaly, primary autosomal recessive.
Dyserythropoietic anemia, congenital, type I.
Muscular dystrophy, limb-girdle, type 2A.
Amyloidosis, hemodialysis-related.
Ceroid-lipofuscinosis, neuronal, late infantile.
Virilization, maternal and fetal.
Carbohydrate-deficient glycoprotein syndrome, type 1b.
Hypercholesterolemia, familial, autosomal recessive.
Retinitis pigmentosa, autosomal recessive.
Here I presented: Victor McKusick, “Mendelian Inheritance in Man”, 1966, Chromosome #15. This print book consists of twelve (12) editions from 1966 to 1998 (shown ABOVE). Selected traits of #15 Chromosome were listed ABOVE. A chromosome is half protein, and half nucleic acid (RNA & DNA). The human body is one (1) percentage nucleic acid (shown BELOW).
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”.
