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Victor McKusick, “Mendelian Inheritance in Man”, 1966. #14 Chromosome.

 


Here I present: Victor McKusick, “Mendelian Inheritance in Man”, 1966. Chromosome #14. This print book  consists of twelve (12) editions from 1966 to 1998 (shown ABOVE). Selected traits of #14 Chromosome are listed BELOW.

Chorea, hereditary benign.    BHC
Meningioma-expressed antigen.    MIA2
Myopathy, distal.   MPD1

Defender against cell death.      DAD1     
Temperature-sensitive apoptosis.        DAD1

Lysinuric protein intolerance.        LPI      

Ichthyosis, lamellar, autosomal recessive.     ARCI1
Ichthyosiform erythroderma, congenital.
Spastic paraplegia.     SPG3A      

Deafness, autosomal recessive.     DFNB35      
Deafness, autosomal dominant.   DFNA23

Meniere disease.       MD
Arrhythmogenic right ventricular dysplasia.
Immunodeficiency.      ARVD1      
Glycogen storage disease.       GSD6    
Phenylketonuria, atypical.      PKU
Dystonia, DOPA-responsive.   DRD
Leber congenital amaurosis, type III.     LCA3    

Tyrosinemia, type Ib.
Alzheimer disease.
Machado-Joseph disease.      MJD
Ovarian cancer.    AKT1
Microphthalmia, autosomal recessive.      MCOP1
Cerebrovascular disease, occlusive.
Leukemia/lymphoma, T-cell.     TCL1A       

Agammaglobulinemia.      AGM1     
Achromatopsia.


Basal ganglia calcification (Fahr disease).

Multinodular goiter.        MNG1
Retinitis pigmentosa, autosomal dominant.     RP27   
Leukemia/lymphoma, T-cell.         TCL1A
Oculopharyngeal muscular dystrophy, autosomal recessive.        OPMD1
APEX nuclease (multifunctional DNA repair enzyme).
Cardiomyopathy, familial hypertrophic.
Oligodontia.
Goiter, familial.
Carbohydrate-deficient glycoprotein syndrome, type II.
Elliptocytosis.
Spherocytosis.
Anemia, neonatal hemolytic, fatal and near-fatal.
Arrhythmogenic right ventricular dysplasia.
Marfan syndrome, atypical.
DNA mismatch repair gene MLH3.
Diabetes mellitus, insulin-dependent.
Krabbe disease.
Hypothyroidism, congenital.
Thyroid adenoma, hyperfunctioning.
Graves disease.
Hyperthyroidism, congenital.
Usher syndrome, autosomal recessive.
Emphysema-cirrhosis.
Hemorrhagic diathesis.
X-Ray repair.


  1. Here I presented: Victor McKusick, “Mendelian Inheritance in Man”, 1966. Chromosome #14.  This print book  consists of twelve (12) editions from 1966 to 1998 (shown ABOVE). Selected traits of #14 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”.

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