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X-linked Mental Retardation
X-linked mental retardation
Overview
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Diseases and disorders
(53)
X-linked mental retardation and macroorchidism
Mental retardation x linked nonspecific
Mental retardation x-linked south african type
Mental retardation
Alpha Thalassemia
Alpha Thalassemia
Alport syndrome
Glycogen storage disease type iib
MASA syndrome
Atr-x syndrome
Lissencephaly
Androgen insensitivity syndrome
Microcephaly
Dysostosis
Limb-girdle
Hunter syndrome
Syndromes
Lesch-nyhan syndrome
Xeroderma pigmentosum variant type
Incontinentia pigmenti
Mucopolysa- ccharidosis
Macroorchidism
Juberg marsidi syndrome
Metabolic syndrome
Pyruvate dehydrogenase deficiency
X-linked sideroblastic anemia
Lowry syndrome
Hypotonia
Macrocephaly
Infantile spasms
Lipid storage disorder
Angelman syndrome
Hypoplasia
X-linked hypophosphatemia
X syndrome
Becker's muscular dystrophy
Anemia, hemolytic
22q11.2 deletion syndrome
Fukuyama type muscular dystrophy
Coffin-lowry syndrome
Myoclonic epilepsy
Lordosis
Skeletal dysplasia
Cornelia de Lange syndrome
Bardet Biedl Syndrome
Agenesis of the corpus callosum
X-linked retinoschisis
Glycogenosis
Growth retardation
Aplasia
Nance-horan syndrome
Menkes disease
Renpenning syndrome
Inborn error of metabolism
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Autism
Rett syndrome
Lujan fryns syndrome
X-linked mental retardation and macroorchidism
Syndromes
(13)
Turner syndrome
X-linked mental retardation and macroorchidism
Alport syndrome
Androgen insensitivity syndrome
Hunter syndrome
Hunter syndrome
Rett syndrome
Lesch-nyhan syndrome
Metabolic syndrome
Lujan fryns syndrome
Infantile spasms
Angelman syndrome
22q11.2 deletion syndrome
Cornelia de Lange syndrome
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Congenital disorders
Genetic disorders
Holoprosencephaly
Lissencephaly
Microcephaly
Macrocephaly
Agenesis of the corpus callosum
Neurological disorders
Aicardi syndrome
Spinocerebellar ataxia
X-linked mental retardation and macroorchidism
Lissencephaly
Infantile spasms
Angelman syndrome
Disability
X-linked mental retardation and macroorchidism
Mental retardation
Spinocerebellar ataxia
Angelman syndrome
Genetics
(8)
X linked
X-linked recessive
Genes
X inactivation
Chromosomes
Chromosomes
Genetic disorder
The Sherman paradox
Genetic disorders
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Lysosomal storage diseases
(40)
Alpha-mannosidosis
Aspartylgl- ucosaminuria
Batten disease
Canavan disease
Cholesteryl ester storage disease
Cholesteryl ester storage disease
Cystinosis
Fabry disease
Farber disease
GM1 gangliosidoses
GM2 gangliosidoses
Galactosialidosis
Gangliosidosis
Gaucher's disease
Glycogen storage disease type iib
Glycoproteinosis
Hunter syndrome
Hurler syndrome
I-cell disease
Krabbe disease
Lipid storage disorder
Lysosomal storage disease
Metachromatic leukodystrophy
Morquio syndrome
Mucolipidosis
Mucolipidosis type IV
Mucopolysa- ccharidosis
Multiple sulfatase deficiency
Neuronal ceroid lipofuscinosis
Niemann-Pick disease, type C
Niemann–Pick disease
Pseudo-Hurler polydystrophy
Pycnodysostosis
Salla disease
Sandhoff disease
Sanfilippo syndrome
Schindler disease
Sialidosis
Sly syndrome
Tay-Sachs disease
Wolman disease
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Genes on chromosome X
Xq28
HSD17B10
JARID1C
OPHN1
ACSL4
Aristaless related homeobox
BRWD3
See also
(20)
FMR1
X-linked dominant
MeCP2
Adrenoleuk- odystrophy
Hyper IgM Syndrome Type 1
Hyper IgM Syndrome Type 1
ATRX
Am. J. Med. Genet.
X chromosome
Adducted
Dysmorphism
Autosomal recessive
Simpson-Go- labi-Behmel syndrome
Genetic counseling
Allan Herndon syndrome
Monosomy
Autosomal dominant
Short stature
SLC9A6
Hypertelorism
Skeletal abnormalities
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