Kosmix
One sec... we're building your guide for
Prader-willi Syndrome
Prader-Willi syndrome
Overview
Tools
Health Providers & Organizations
Main ›
Tools ›
Health Providers & Organizations ›
Tools
›
Skinsight
Body Location Disease Search
Related in the Kosmos
?
Disability
Angelman syndrome
Congenital disorders
Hypomentia
Fragile x syndrome
Developmental delay
Syndromes
(27)
Smith-Magenis syndrome
Williams syndrome
Cri du chat syndrome
Wolf-Hirschhorn syndrome
Turner syndrome
Turner syndrome
22q11.2 deletion syndrome
Rett syndrome
Noonan syndrome
Proteus syndrome
Lesch-nyhan syndrome
Klinefelter syndrome
Sanfilippo syndrome
Russell-Silver syndrome
Peutz-jeghers syndrome
Fetofetal transfusion
Trisomy 13
Cornelia de Lange syndrome
Testicular feminization
Stickler syndrome
Syndrome
WAGR complex
Windmill-Vane-Hand syndrome
Congenital rubella
Alagille syndrome
Edwards syndrome
Angelman syndrome
Fragile x syndrome
more...
Genetic disorders
(36)
Aicardi syndrome
Bardet Biedl Syndrome
Microdeletion
Disomy
Smith-lemli-opitz syndrome
Smith-lemli-opitz syndrome
Canavan disease
Pseudoxanthoma elasticum
Chromosome abnormality
Metachromatic leukodystrophy
Glutaricaciduria
Rubinstein-taybi syndrome
Popliteal pterygium syndrome
Shwachman syndrome
Monosomies
Phenylketonuria
Angelman syndrome
Smith-Magenis syndrome
Williams syndrome
Cri du chat syndrome
Wolf-Hirschhorn syndrome
Turner syndrome
Fragile x syndrome
22q11.2 deletion syndrome
Rett syndrome
Noonan syndrome
Lesch-nyhan syndrome
Klinefelter syndrome
Sanfilippo syndrome
Peutz-jeghers syndrome
Trisomy 13
Cornelia de Lange syndrome
Testicular feminization
Stickler syndrome
WAGR complex
Alagille syndrome
Edwards syndrome
more...
Medical condition
(47)
Pseudochol- inesterase deficiency
Hypotonia
Labhart-willi syndrome
Uniparental disomy
Gonadal dysgenesis
Gonadal dysgenesis
Froelich's syndrome
Hypogonadotropic hypogonadism
Growth hormone deficiency
Feeding difficulties
Craniofrontonasal dysplasia
Polyglucosan body disease adult
Floating harbor syndrome
Progressive osseous heteroplasia
Small for gestational age
Wildervanck syndrome
Undescended testicles
Progressive supranuclear palsy
Craniopharyngioma
Angelman syndrome
Bardet Biedl Syndrome
Cri du chat syndrome
Hypomentia
Disomy
Fragile x syndrome
22q11.2 deletion syndrome
Noonan syndrome
Proteus syndrome
Canavan disease
Lesch-nyhan syndrome
Klinefelter syndrome
Sanfilippo syndrome
Pseudoxanthoma elasticum
Fetofetal transfusion
Trisomy 13
Chromosome abnormality
Cornelia de Lange syndrome
Testicular feminization
Metachromatic leukodystrophy
Glutaricaciduria
Popliteal pterygium syndrome
Stickler syndrome
Shwachman syndrome
WAGR complex
Windmill-Vane-Hand syndrome
Alagille syndrome
Phenylketonuria
Edwards syndrome
more...
Rare diseases
(10)
Angelman syndrome
Williams syndrome
Cri du chat syndrome
Proteus syndrome
Lesch-nyhan syndrome
Lesch-nyhan syndrome
Sanfilippo syndrome
Metachromatic leukodystrophy
Popliteal pterygium syndrome
Stickler syndrome
Alagille syndrome
more...
Genetics
Genomic imprinting
Contiguous gene syndrome
Angelman syndrome
Uniparental disomy
Congenital disorders
Genetic disorders
Microdeletion
Pediatrics
Growth hormone treatment
Delayed puberty
Fragile x syndrome
Lesch-nyhan syndrome
Small for gestational age
Shwachman syndrome
Alagille syndrome
Cytogenetics
(20)
Autosome
Chromosomal translocation
Chromosome
Chromosome abnormality
Colcemid
Colcemid
Disomy
Fluorescent in situ hybridization
Fragile sites
Germ plasm
Homologous chromosome
Karyotype
Monosomies
Ploidy
Pseudoautosomal region
Robertsonian translocation
Synapsis
Tetrasomy
Trisomy
Uniparental disomy
X chromosome
more...
Diseases and disorders
Post-infectious glomerulonephritis
Hyperphagia
Growth failure
Metachromatic leukodystrophy
Symptoms
(15)
Premenstrual tenderness and swelling
Decreased muscle tone
Delayed development
Skeletal (limb) abnormalities
Stretch marks
Stretch marks
Hypotonia
Hyperphagia
Short stature
Hypomentia
Growth failure
Primary amenorrhea
Feeding difficulties
Undescended testicles
Developmental delay
Delayed puberty
more...
Signs and tests
Chronic
Glucose tolerance test
Hypercapnia
Hyperinsulinism
Luteinizing hormone
Hypotonia
Causes, incidence, and risk factors
Cor pulmonale
Hypoxia
Respiratory system
Chromosome
See also
(20)
Diseases and disorders
Chromosome 15
Pseudo-ainhum
Pwsa
Norditropin
Norditropin
Short stature
Particle velocity
Poison control centers
Skin picking
SNRPN
TNFR
Genes on chromosome 15
Paternally
Fan-fold
UBE3A
Primary amenorrhea
Diabetes mellitus
Epigenetics
Juan Carreño de Miranda
Obesity
more...
more categories...
Health Providers & Organizations
›
Vitals.com
