Here I present: Victor McKusick, “Mendelian Inheritance in Man”, 1966, Chromosome #21. This print book consists of twelve (12) editions from 1966 to 1998 shown ABOVE.
Thirty (30) alleles contained on chromosome #21 are listed BELOW.
Region 21p1 Traits.
Coxsackie and adenovirus receptor. CXADR
Amyloidsis, cerebroarterial, Dutch-type. CAA
Alzheimer disease, APP-related. AD1
Schizophrenia, chronic. SCZD
Usher syndrome, autosomal recessive. USH1
Amytrophic lateral sclerosis. ALS1
Jervell and Lange-Nielsen syndrome. JLNS1
Long QT syndrome. LQT1
Down syndrome cell adhesion molecule. DSCAM
Region 21q1 Traits.
Homocystinuria. CBS
Cataract, congenital, autosomal dominant. CATC1
Deafness, autosomal recessive. DFNB98
Myxovirus (influenza) resistance. MX1
Myeloproliferative syndrome, transient. MST
Leukemia, transient, of Down syndrome. TAM
Enterokinase deficiency. PRSS7
Multiple carboxylase deficiency. HLCS
T-cell lymphoma invasion and metastasis. TIAM1
Region 21q2 Traits.
Mycobacterial infection, atypical. IMD27A
Down syndrome (critical region). DCR
Autoimmune polyglandular disease, type 1. APS1
Bethlem myopathy. BTHLM1A
Epilepsy, progressive myoclonic. EPM1
Holoprosencephaly, alobar. HPE1
Knobloch syndrome. KNO1
Breast cancer. TTF1
Platelet disorder, with myeloid malignancy. FPDMM
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”.
