Here I present: Victor McKusick, “Mendelian Inheritance in Man”, 1966. Chromosome #X. This print book consists of twelve (12) editions from 1966 to 1998 (shown ABOVE ). The following abbreviations may used for Chromosome #X traits, listed in alphabetical order. AIS ALD AR BMP15 BRS3 BTK CACNA1 CBD CLCN5 DMD DKCX DYX9 ED1 FMR1 … Continue reading Victor McKusick, “Mendelian Inheritance in Man”, 1966. Chromosome #X.
Cholesterol-lowering factor. CLF
Deafness, autosomal dominant and recessive. DFNA84
Vohwinkel syndrome. VOWNKL
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
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
Rhabdomyosarcoma, alveolar. RMS2
Lung cancer, non small-cell. NSCLC
Spinocerebellar ataxia. SCA27A
Ceroid-lipofuscinosis, neonatal. CLN5
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”.
Continue reading “Victor McKusick, “Mendelian Inheritance in Man”, 1966. Chromosome #13.”
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 Hepatocellular carcinoma. … Continue reading Victor McKusick, “Mendelian Inheritance in Man”, 1966, Chromosome #16.
