Here I present: Victor McKusick, “Mendelian Inheritance in Man”, 1966, Chromosome #22. This book was printed in twelve (12) editions from 1966 to 1998 shown ABOVE.
The following abbreviations may used for Chromosome #22 traits, listed in alphabetical order.
Chromosome 22.
ALS1 COMT CSF2RB EWSR FLD1 GPR24 HPS IGLC1 MYH9 PDGFB PPARA
SLC5A1 SOX10 TBX1
Thrombophilia. THPH10
Rhabdoid predisposition syndrome, familial. RTPS1
Giant platelet disorder, isolated. GP1BB
Hyperprolinemia. HRPRO1
Cataract, cerulean, type 2. CTRCT3
Leukemia, chronic myeloid. CML
Neuroepithelioma. PNE
Fechtner syndrome. FTNS
Amyotrophic lateral sclerosis. ALS1
Pulmonary alveolar proteinosis. SMDP4
Dermatofibrosarcoma protuberans. DFSP
Giant-cell fibroblastoma. DFSP
Spinocerebellar ataxia. SCA10
Waardenburg-Shah syndrome. WS2E
Yemenite deaf-blind hypopigmentation syndrome. SOX10
Debrisoquine sensitivity. CYP2D6
Polycystic kidney disease. PKD
Leukodystrophy, metachromatic. MLD
Myoneurogastrointestinal encephalopathy. MTDPS1
Leukoencephalopathy. MLC1
DiGeorge syndrome. DGS2
Region 22q1 Traits.
Velocardiofacial syndrome. VCFS
Schindler disease. NAGA
Kanzaki disease. NAGA
Epilepsy, partial. FFEVF1
Glutathioninuria. GSSD
Opitz G syndrome, type II. GBBB
Ubiquitin fusion degradation. UFD1L
Transcobalamin deficiency. TCN2D
Heme oxygenase deficiency. HMOX1D
Manic Fringe. LFNG
Leukemia inhibitory factor. LIF
Neurofibromatosis, type 2. NF2
Meningioma, NF2-related, sporadic. NF2
Neurolemmomatosis. NF1
Malignant mesothelioma, sporadic. MESOM
Deafness, autosomal dominant. DFNA17
Cardioencephalomyopathy, fatal infantile. MC4DN2
Adenylosuccinase deficiency. ADSLD
Autism, succinylpurinemic. ADSLD
Glucose/Galactose malabsorption. GGM
Benzodiazepine receptor, peripheral type. BZRP
Methemoglobinemia, types I and II. CYB5R3
- Here I presented: Victor McKusick, “Mendelian Inheritance in Man”, 1966, Chromosome #22. There are fifty-three (53) alleles of chromosome #22 listed ABOVE.
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”.
