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Male Turner Syndrome
Male turner syndrome
Overview
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Diseases and disorders
(62)
Klinefelter syndrome
Noonan syndrome
Androgen insensitivity syndrome
Webbing of neck
Aneuploidy
Aneuploidy
Intersexuality
XX male syndrome
Chromosomal abnormality
Morvan disease
Growth hormone deficiency
Congenital adrenal hyperplasia
Hypogonadotropic hypogonadism
Glossopharyngeal nerve diseases
Hyperostosis, cortical, congenital
Hypospadias
Growth failure
Fukuyama type muscular dystrophy
Multiple hamartoma syndrome
Marinesco sjogren syndrome
Purpura, schoenlein-henoch
Type i complex regional pain syndrome
Myopathies, structural, congenital
XYY
Enterocolitis, pseudomembranous
Hereditary sensory and autonomic neuropathies
Leukodystrophy, globoid cell
Physiologic nystagmus
Mixed gonadal dysgenesis
Fetofetal transfusion
Histiocytosis non-langerhans-cell
Streak gonads
Polyploidy
Swyer syndrome
Lupus erythematosus, cutaneous
Polyendocr- inopathies, autoimmune
Postpoliomyelitis syndrome
Encephalitis, arbovirus
Olfaction disorders
Metatropic dwarfism
Prader Willi syndrome
Undescended testicles
Monosomy x
47,XY,+21
Turner-like syndrome
Intervertebral disk displacement
Trisomy 22
Aplasia
Pectus excavatum
Rosenthal syndrome
Hyperprolactinemia
Premature ovarian failure
Triple X syndrome
Hermaphroditism
Cri du chat
Mayer-Roki- tansky-Kuster-Hauser syndrome
Trisomy 9
Galactosemias
Fragile x syndrome
Trisomy 18
Thymic aplasia
Brachial plexus neuropathies
Constitutional delay
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Endocrinology
Turner syndrome
5 alpha reductase deficiency
Sertoli cell-only syndrome
Congenital adrenal hyperplasia
Hypogonadotropic hypogonadism
Polyendocr- inopathies, autoimmune
Premature ovarian failure
Syndromes
(18)
Treacher Collins syndrome
Turner syndrome
Klinefelter syndrome
Noonan syndrome
Androgen insensitivity syndrome
Androgen insensitivity syndrome
XYY
Hereditary sensory and autonomic neuropathies
Fetofetal transfusion
Swyer syndrome
Prader Willi syndrome
47,XY,+21
Triple X syndrome
Cri du chat
Mayer-Roki- tansky-Kuster-Hauser syndrome
Fragile x syndrome
Trisomy 18
Thymic aplasia
Sertoli cell-only syndrome
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Genodermatoses
Turner syndrome
Klinefelter syndrome
Noonan syndrome
Treacher Collins syndrome
Genetics
Mosaicism
Chromosomes
Genetic disorders
X linked
XX male syndrome
XYY
Sex
Sex chromosome
Sexual differentiation
Hermaphroditism
Cytogenetics
(20)
Autosomes
Chromosome
Haploidisation
Karyotype
Monosomy
Monosomy
Translocations
X chromosomes
Aneuploidy
Chromosomal abnormality
Colcemid
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Homologous chromosome
Pseudoautosomal region
Robertsonian translocation
Synapsis
Tetrasomy
Trisomy
Uniparental disomy
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Chromosomes
(57)
Y chromosome
AZF1
Allosome
Autosomes
Centromere
Centromere
Chromatid
Chromomere
Chromosomal abnormality
Chromosomal inversion
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
Satellite chromosome
Small supernumerary marker chromosome
Subtelomere
Syntelic
Telomere
Translocations
X chromosomes
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Reproductive system
Gonadal
Ovo-testes
Secondary sexual characteristics
Gametes
Hypogonadotropic hypogonadism
Human body
Hypothalamic
Trabecular bone
Epiphyses
Brachial plexus neuropathies
Intersexuality
(28)
Progestin induced virilization
17-beta-hy- droxysteroid dehydrogenase deficiency
5 alpha reductase deficiency
Androgen insensitivity syndrome
Androgen-induced hermaphroditism
Androgen-induced hermaphroditism
Breast binding
Congenital adrenal hyperplasia
Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
Congenital adrenal hyperplasia due to 3 beta-hydroxysteroid dehydrogenase deficiency
Genital reconstructive surgery
Hermaphroditism
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
Pseudoherm- aphroditism
Sex assignment
Streak gonads
Swyer syndrome
Trans March
Transcending Boundaries Conference
True hermaphroditism
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See also
(15)
Short stature
External genitalia
Am. J. Med. Genet.
PTPN11
Adrenoleuk- odystrophy
Adrenoleuk- odystrophy
Haplo-diploid sex-determination system
Mullerian inhibiting factor
Jacqueline Noonan
Trisomy 21
Chimerism
Somatropin
SRY gene
49, XXXXX
Wide set eyes
IGF-I
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