Here I present: Victor McKusick, “Mendelian Inheritance in Man”, 1966, Chromosome #17. Selected traits of chromosome #17 are listed BELOW.
Region 17p1 Traits.
Diabetes mellitus, noninsulin-dependent.
Deafness, autosomal recessive.
Maturity Onset Diabetes of the Young, type V.
Hypertension, essential, susceptibility to.
T-cell immunodeficiency, alopecia, and nail dystrophy.
Chondrosarcoma, extraskeletal myxoid.
Neurotransmitter transporter, serotonin (anxiety-related).
Leukemia, juvenile myelomonocytic.
HIV-1 disease, delayed progression of.
Muscular dystrophy, limb-girdle.
Epidermolysis bullosa simplex, recessive.
Pachyonychia congenita, Jackson-Lawler type.
Glycogen storage disease (von Gierke disease).
Patella aplasia or hypoplasia.
Region 17q1 Traits.
Ehlers-Danlos syndrome, types I and VIIA.
Glanzmann thrombasthenia, type A.
Thrombocytopenia, neonatal alloimmune.
Myocardial infarction, susceptibility to.
Alzheimer disease, susceptibility to.
Campomelic dysplasia with autosomal sex reversal.
Breast cancer-related regulator of TP53.
Subcortical laminar heterotopia.
Leber congenital amaurosis, type I.
Myasthenia gravis, familial infantile.
Charcot-Marie tooth neuropathy.
Van der Woude syndrome modifier.
Choroidal dystrophy, central areolar.
Region 17q2 Traits.
Huntingtin-associated protein.
Alzheimer disease, susceptibility to.
Malignant hyperthermia susceptibility.
Leukemia, acute promyelocytic.
Epidermolytic palmoplantar keratoderma.
Pachyonychia congenita, Jadassohn-Lewandowsky type.
Keratoderma, nonepidermolytic palmoplantar.
Muscular dystrophy, Duchenne-like, type 2.
Leukemia, myeloid/lymphoid or mixed-lineage.
Gliosis, familial progressive subcortical.
Pseudohypoaldosteronism type II.
Renal tubular acidosis, distal.
T-cell leukemia (I and II) receptor.
Dementia, frontotemporal, with Parkinsonism.
Glanzmann thrombasthenia, type B.
Tylosis with esophageal cancer.
Adrenoleukodystrophy, pseudoneonatal.
Leukemia, acute myeloid, therapy-related.
Myasthenic syndrome, slow-channel congenital.
Sanfilippo syndrome, types A and B.
Here I presented: Victor McKusick, “Mendelian Inheritance in Man”, 1966, Chromosome #17. Selected traits of chromosome #17 are 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”.
