Victor McKusick, “Mendelian Inheritance in Man”, 1966. Chromosome #13.

Here I present: Victor McKusick, “Mendelian Inheritance in Man”, 1966. Chromosome #13. This print book consists of twelve (12) editions from 1966 to 1998 (shown ABOVE). Selected traits of #13 Chromosome are listed BELOW.

Cholesterol-lowering factor. CLF

Deafness, autosomal dominant and recessive. DFNA84

Vohwinkel syndrome. VOWNKL

Ectodermal dysplasia. ED2

Muscular dystrophy, limb-girdle, type 2C. LGMDR5

Breast cancer, early onset. BRCA2

Pancreatic cancer. PNCA2

Disrupted in B-cell neoplasia. DBM

Leukemia, chronic lymphocytic, B-cell. CLLS2

MHC class II deficiency, group B. MHC

Hyperornithinemia, hyperammonemia, homocitrullinuria. HHH

Serotonin receptor. HTR2

Retinoblastoma. RB1

Osteosarcoma. OSRC

Bladder cancer. RB1

Pinealoma with bilateral retinoblastoma. RB1

Wilson disease. WD

Postaxial polydactyly, type A2. PAPA2

Hirschsprung disease. HSCR2

Propionic Acidemia, type I or pccA. PCCA

Holoprosencephaly. HPE5

Bile acid malabsorption, primary. PBAM

Cataract, zonular pulverulent. CZP3

Stem-cell leukemia/lymphoma syndrome. AML

Spastic ataxia, Charlevoix-Saguenay type. SACS

Pancreatic agenesis. PAGEN1

Maturity Onset Diabetes of the Young, type IV. MODY4

Enuresis, nocturnal. ENUR1

Dementia, familial British. FBD

Rieger syndrome, type 2. RIEG2

X-Ray sensitivity. XRS

Rhabdomyosarcoma, alveolar. RMS2

Lung cancer, non small-cell. NSCLC

Spinocerebellar ataxia. SCA27A

Ceroid-lipofuscinosis, neonatal. CLN5

Microcoria, congenital. MCOR

Schizophrenia susceptibility. SCZD

Xeroderma pigmentosum, group G. XPG

Coagulation Factor VII deficiency. F7

Oguchi disease. GPRK1

Stargardt disease, autosomal dominant. STGD3

Coagulation Factor X deficiency. F10

Breast cancer, ductal. BRCA2

Here I presented: Victor McKusick, “Mendelian Inheritance in Man”, 1966. Chromosome #13. This print book consists of twelve (12) editions from 1966 to 1998 (shown ABOVE). Selected traits of #13 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”.