Here I present: Victor McKusick, “Mendelian Inheritance in Man”, 1966, #16 Chromosome. This print book consists of twelve (12) editions from 1966 to 1998 (shown ABOVE). Selected traits of #16 Chromosome are listed BELOW.
Region 16p1 Traits.
Methemoglobinemia, alpha. HBA1
Erythemias, alpha. HBA2
Heinz body anemias, alpha. HBA2
Alpha-thalassemia/mental retardation. HBHR
Axis inhibitor. AXIN
Rubinstein-Taybi syndrome. RSTS1
Tuberous sclerosis. TSC2
Polycystic kidney disease, adult type I. PKD1
Leukemia, acute myelomonocytic. AML
Epilepsy, myoclonic, infantile. FIME
MHC class II deficiency. CIITA
Atopy, susceptibility to. IGER
Glycogenosis, hepatic, autosomal. GSD9B
Medullary cystic kidney disease, autosomal dominant. ADTKD1
Convulsions, infantile and paroxysmal choreoathetosis. ICCA
Arthrocutaneouveal granulomatosis (Blau syndrome). NOD2
Paroxysmal kinesigenic choreoathetosis. PKC
Wilms tumor. WT3
Hypodontia, autosomal recessive. HYD2
Cocaine- and antidepressant-sensitive. SLC6A2
Orthostatic intolerance. SLC6A2
Leukemia, acute myelogenous. AML
Macular dystrophy, corneal. MCD
Region 16q1 Traits.
Norum disease. LCAT
Fish-eye disease. LCAT
Tyrosinemia, type II. TYRSN2
Breast cancer antiestrogen resistance. BCAR4
Fibrosis of extraocular muscles congenital. FEOM3
Fanconi anemia, complementation group A. FANCA
Lymphedema with distichiasis. LPHDST
Spastic paraplegia. SPG89
Chronic granulomatous disease, autosomal. CGD4
Urolithiasis, 2,8-dihydroxyadenine. APRTD
Mucopolysaccharidosis. MPS4A
UV-induced skin damage, vulnerability to. CMM5
Erthrocytosis. ECYT7
Hypochromic microcytic anemia. HBHT
GABA-transaminase deficiency. GABATD
Cataract, congenital, with microphthalmia. MCOPCT1
Polycystic kidney disease, infantile severe. PKDTS
Ubiquitin-specific protease, herpes virus-associated. USP7
Xeroderma pigmentosum, group F. XP6
Microhydranencephaly. MHAC
Tamm-Horsfall glycoprotein. THGP
Cerebellar degeneration-related antigen. CDR2
Familial Mediterranean fever. FMF
Region 16q2 Traits.
Liddle syndrome. LIDLS1
Pseudohypoaldosteronism, type I. PHA1B3
Batten disease. CLN3
Mitral vavle prolapse, familial. MVP1
Brody myopathy. BROD
Retinoblastoma-binding protein. RBBP6
Inflammatory bowel disease (Crohn disease). IBD1
Myxoid liposarcoma, fusion gene in. STX1B
Cylindromatosis, familial. CYLD
Townes-Brocks syndrome. TBS1
Retinoblastoma. RB2
Gitelman syndrome. GTLMNS
Leukemia, acute myeloid, M4Eo subtype. AML
Ras-related gene associated with diabetes. RRAD
Ovarian carcinoma. CDH1
Gastric cancer, familial. HDGC
Benzene toxicity, susceptibility to. NQO1
Leukemia, postchemotherapy, susceptibility to. NQO1
Spinocerebellar ataxia. SCAR16
Stomatocytosis, dehydrated hereditary. DHS
Pseudohyperkalemia, familial. DHS
Here I presented: Victor McKusick, “Mendelian Inheritance in Man”, 1966, #16 Chromosome. This print book consists of twelve (12) editions from 1966 to 1998 (shown ABOVE). Selected traits of #16 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”.
