Victor McKusick, “Mendelian Inheritance in Man”, 1966, Chromosome #17.

Here I present: Victor McKusick, “Mendelian Inheritance in Man”, 1966, Chromosome #17. Selected traits of chromosome #17 are listed BELOW.

Region 17p1 Traits.

Canavan disease.

Ovarian cancer.

Miller-Dieker syndrome.

Retinitis pigmentosa.

Tumor protein.

Colorectal cancer.

Li-Fraumeni syndrome.

Cystinosis, nephropathic.

Diabetes mellitus, noninsulin-dependent.

Cone dystrophy.

Myasthenic syndrome.

Deafness, autosomal recessive.

Smith-Magenis syndrome.

VLCAD deficiency.

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).

Neurofibromatosis, type 1.

Watson syndrome.

Leukemia, juvenile myelomonocytic.

HIV-1 disease, delayed progression of.

Meesmann corneal dystrophy.

Muscular dystrophy, limb-girdle.

Epidermolysis bullosa simplex, recessive.

Pachyonychia congenita, Jackson-Lawler type.

Steatocustoma multiplex.

Wilms tumor, type 4.

Glycogen storage disease (von Gierke disease).

Parkinsonism-dementia.

Epidermolysis hyperkeratosis.

Patella aplasia or hypoplasia.

Osteogenesis imperfecta.

Region 17q1 Traits.

Ehlers-Danlos syndrome, types I and VIIA.

Osteoporosis, idiopathic.

Ovarian carcinoma antigen.

Neuroblastoma.

Glanzmann thrombasthenia, type A.

Thrombocytopenia, neonatal alloimmune.

CLL/lymphoma, B-cell.

Retinitis pigmentosa.

Pituitary tumor, invasive.

Myocardial infarction, susceptibility to.

Alzheimer disease, susceptibility to.

Myotonia congenita, atypical. 

Cramps, familial.

Fetal Alzheimer antigen.

Lung cancer, small-cell.

Campomelic dysplasia with autosomal sex reversal.

Apoptosis inhibitor.

Diabetes mellitus, type II.

Radical fringe.

Bernard-Soulier Syndrome.

Breast cancer-related regulator of TP53.

Hypermethylated in cancer.

Lissencephaly.

Subcortical laminar heterotopia.

Leber congenital amaurosis, type I.

Medulloblastoma.

Cataract, anterior polar.

Myasthenia gravis, familial infantile.

Bruck syndrome.

Sjogren-Larsson syndrome.

Charcot-Marie tooth neuropathy.

Dejerine-Sottas disease.

Van der Woude syndrome modifier.

Choroidal dystrophy, central areolar.

Region 17q2 Traits.

Huntingtin-associated protein.

Psoriasis susceptibility.

Epidermolysis bullosa.

Alzheimer disease, susceptibility to.

Van Buchenwald’s disease.

Malignant hyperthermia susceptibility.

Leukemia, acute promyelocytic.

Epidermolytic palmoplantar keratoderma.

Pachyonychia congenita, Jadassohn-Lewandowsky type.

Keratoderma, nonepidermolytic palmoplantar.

Sclerosteosis.

Muscular dystrophy, Duchenne-like, type 2.

Adhalinopathy, primary.

Breast cancer, early onset.

Ovarian cancer.

Leukemia, myeloid/lymphoid or mixed-lineage.

Gliosis, familial progressive subcortical.

Pseudohypoaldosteronism type II.

Spherocytosis, hereditary.

Hemolytic anemia.

Renal tubular acidosis, distal.

T-cell leukemia (I and II) receptor.

Dementia, frontotemporal, with Parkinsonism.

Trichodontoosseous syndrome.

Glanzmann thrombasthenia, type B.

Symphalangism, proximal.

Mulibrey nanism.

Growth hormone deficiency.

Myeloperoxidase deficiency.

Cataracts.

Tylosis with esophageal cancer.

Adrenoleukodystrophy, pseudoneonatal.

Deafness, autosomal dominant.

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”.