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Turner-like Syndrome
Turner-like syndrome
Overview
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Diseases and disorders
(67)
Tracheoesophageal fistula
Persistent truncus arteriosus
Hyperlipop- roteinemia type I
Trichiniasis
Tuberculosis
Tuberculosis
Transposition of great vessels
Noonan syndrome
Neonatal hyperbilirubinemia
Tricuspid atresia
Klinefelter syndrome
Webbing of neck
XX male syndrome
Glossopharyngeal nerve diseases
Prader Willi syndrome
Hyperostosis, cortical, congenital
Pectus excavatum
Fukuyama type muscular dystrophy
Undescended testicles
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
Craniopharyngioma
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Physiologic nystagmus
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Enterocolitis, pseudomembranous
Thoracic celosomia
Tyrosine-oxidase temporary deficiency
Growth failure
Gonadal dysgenesis
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Growth hormone deficiency
Morvan disease
Chromosomal abnormality
Intervertebral disk displacement
Rosenthal syndrome
Metatropic dwarfism
True hermaphroditism
Monosomy x
Male turner syndrome
Aneuploidy
Galactosemias
Androgen insensitivity syndrome
Brachial plexus neuropathies
Multiple sulfatase deficiency
Vaginal septum
Trisomy 13
Aplasia
Optic neuropathy, ischemic
Neurofibro- matosis-noonan syndrome
Cystic hygroma
Trisomy 18
Macrocephaly
Pulmonary stenosis
Ambiguous genitalia
XYY
Aniridia
Marinesco sjogren syndrome
Adrenogenital syndrome
Juvenile primary lateral sclerosis
Swyer syndrome
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Genodermatoses
Turner syndrome
Noonan syndrome
Klinefelter syndrome
Multiple sulfatase deficiency
Neurofibro- matosis-noonan syndrome
Syndromes
(11)
Turner syndrome
Noonan syndrome
Klinefelter syndrome
Prader Willi syndrome
Hereditary sensory and autonomic neuropathies
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
Androgen insensitivity syndrome
Trisomy 13
Trisomy 18
XYY
Swyer syndrome
more...
Genetic disorders
(20)
Monosomy
Adrenoleuk- odystrophy
Turner syndrome
Noonan syndrome
Klinefelter syndrome
Klinefelter syndrome
XX male syndrome
Prader Willi syndrome
Hyperostosis, cortical, congenital
Fukuyama type muscular dystrophy
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Chromosomal abnormality
Aneuploidy
Galactosemias
Androgen insensitivity syndrome
Multiple sulfatase deficiency
Trisomy 13
Trisomy 18
XYY
Adrenogenital syndrome
more...
Intersexuality
(28)
17-beta-hy- droxysteroid dehydrogenase deficiency
5-alpha-reductase deficiency
Adrenogenital syndrome
Androgen insensitivity syndrome
Androgen-induced hermaphroditism
Androgen-induced hermaphroditism
Breast binding
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency
Genital reconstructive surgery
Gonadal dysgenesis
Hermaphrodite
Hermaphroditus
Imposex
Intersex Society of North America
Intersex people
Intersexuality (Conditions)
Intersexuality (Disorders of sex development)
Klinefelter syndrome
Lipoid congenital adrenal hyperplasia
Mixed gonadal dysgenesis
Organisation Intersex International
Progestin-induced virilisation
Pseudoherm- aphroditism
Sex assignment
Swyer syndrome
Trans March
Transcending Boundaries Conference
True hermaphroditism
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Cytogenetics
(20)
Autosomes
Karyotype
X chromosome
Aneuploidy
Chromosomal abnormality
Chromosomal abnormality
Chromosomal translocation
Chromosome
Colcemid
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Homologous chromosome
Monosomy
Ploidy
Pseudoautosomal region
Robertsonian translocation
Synapsis
Tetrasomy
Trisomy
Uniparental disomy
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Chromosomes
(57)
Centromere
Chromatids
Satellite chromosome
Y chromosomes
AZF1
AZF1
Allosome
Autosomes
Chromomere
Chromosomal abnormality
Chromosomal inversion
Chromosomal translocation
Chromosome
Chromosome 1 (human)
Chromosome 10 (human)
Chromosome 11 (human)
Chromosome 12 (human)
Chromosome 13 (human)
Chromosome 14 (human)
Chromosome 15 (human)
Chromosome 16 (human)
Chromosome 17 (human)
Chromosome 18 (human)
Chromosome 19 (human)
Chromosome 2 (human)
Chromosome 20 (human)
Chromosome 21 (human)
Chromosome 22 (human)
Chromosome 3 (human)
Chromosome 4 (human)
Chromosome 5 (human)
Chromosome 6 (human)
Chromosome 7 (human)
Chromosome 8 (human)
Chromosome 9 (human)
Chromosome conformation capture
Chromosome engineering
Chromosome regions
Chromosome segregation
Derivative chromosome
Dicentric chromosome
Dyad (biology)
G banding
Human β-globin locus
Inchrosil
Isochromosome
Karyotype
Lampbrush chromosome
Locus (genetics)
Marker chromosome
Personalized medicine
Proline-Rich Coiled Coil 1
Ring chromosome
Small supernumerary marker chromosome
Subtelomere
Syntelic
Telomere
X chromosome
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Symptoms
Short stature
Wide set eyes
Swollen hands
Undescended testicles
Growth failure
Delayed puberty
See also
(18)
Transtentorial herniation
Tongue inflammation
Sex chromosomes
PTPN11
Mosaicism
Mosaicism
Chromosome (genetic algorithm)
Heterochromatin
Prenatal diagnosis
Somatropin
Norditropin
Holoprosencephaly
Delayed puberty
Mycosis fungoides
Cyanotic
Imperforate hymen
IGF-I
Mullerian duct
MAGIC Foundation
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