Pages that link to "X-linked recessive inheritance"
From WikiMD's Wellness Encyclopedia
The following pages link to X-linked recessive inheritance:
Displaying 22 items.
- UBA1 (← links | edit)
- Retinoschisin (← links | edit)
- SMC1A (← links | edit)
- Emery's rule (← links | edit)
- Ogden syndrome (← links | edit)
- DDX3X syndrome (← links | edit)
- Wieacker syndrome (← links | edit)
- Chudley–Lowry–Hoar syndrome (← links | edit)
- Waaler–Aarskog syndrome (← links | edit)
- XMEN disease (← links | edit)
- Allan Herndon Dudley syndrome (← links | edit)
- John Menkes (← links | edit)
- Short-stature homeobox gene (← links | edit)
- Blue-cone monochromacy (← links | edit)
- Adrenoleukodystrophy (← links | edit)
- Albinism–deafness syndrome (← links | edit)
- X-linked recessive (redirect page) (← links | edit)
- Lymphedema (← links | edit)
- Myasthenia gravis (← links | edit)
- Incontinentia pigmenti (← links | edit)
- Neuromyotonia (← links | edit)
- Aarskog–Scott syndrome (← links | edit)
- Hypotonia (← links | edit)
- Hypertonia (← links | edit)
- Autosomal dominant (← links | edit)
- Duchenne muscular dystrophy (← links | edit)
- Ichthyosis (← links | edit)
- Leukodystrophy (← links | edit)
- Bloom syndrome (← links | edit)
- Glucose-6-phosphate dehydrogenase deficiency (← links | edit)
- Androgen insensitivity syndrome (← links | edit)
- Aplasia cutis congenita (← links | edit)
- Barth syndrome (← links | edit)
- Epstein syndrome (← links | edit)
- Fabry disease (← links | edit)
- Fanconi anemia (← links | edit)
- Myotonic dystrophy (← links | edit)
- Oculocerebrorenal syndrome (← links | edit)
- Palmoplantar keratoderma (← links | edit)
- X-linked adrenal hypoplasia congenita (← links | edit)
- Chronic granulomatous disease (← links | edit)
- X-linked agammaglobulinemia (← links | edit)
- Mastocytosis (← links | edit)
- ABCD syndrome (← links | edit)
- Dichromatism (← links | edit)
- Periodic paralysis (← links | edit)
- Cutis laxa (← links | edit)
- Fields' disease (← links | edit)
- Thyrotoxic myopathy (← links | edit)
- Mohr–Tranebjærg syndrome (← links | edit)
- Abruzzo–Erickson syndrome (← links | edit)
- X-linked spinal muscular atrophy type 2 (← links | edit)
- Aldred syndrome (← links | edit)
- Myopathy, X-linked, with excessive autophagy (← links | edit)
- Pelizaeus–Merzbacher disease (← links | edit)
- Simpson–Golabi–Behmel syndrome (← links | edit)
- Sjögren–Larsson syndrome (← links | edit)
- Smith–Fineman–Myers syndrome (← links | edit)
- Walker–Warburg syndrome (← links | edit)
- Wiskott–Aldrich syndrome (← links | edit)
- X-linked dystonia parkinsonism (← links | edit)
- X-linked endothelial corneal dystrophy (← links | edit)
- X-linked myotubular myopathy (← links | edit)
- X-linked recessive hypoparathyroidism (← links | edit)
- Bloch-sulzberger syndrome (← links | edit)
- Congenital myopathy (← links | edit)
- Glycogen storage disease (← links | edit)
- Becker muscular dystrophy (← links | edit)
- Bethlem myopathy (← links | edit)
- Biemond syndrome (← links | edit)
- Birk-Barel syndrome (← links | edit)
- Blue diaper syndrome (← links | edit)
- Xeroderma pigmentosum (← links | edit)
- Spinal and bulbar muscular atrophy (← links | edit)
- Stickler syndrome (← links | edit)
- Ocular albinism type 1 (← links | edit)
- Ornithine transcarbamylase deficiency (← links | edit)
- L1 syndrome (← links | edit)
- Lenz microphthalmia syndrome (← links | edit)
- Kallmann syndrome (← links | edit)
- FG syndrome (← links | edit)
- Focal dermal hypoplasia (← links | edit)
- Epidermolysis bullosa (← links | edit)
- Epidermolysis bullosa simplex (← links | edit)
- Dyskeratosis congenita (← links | edit)
- Chronic progressive external ophthalmoplegia (← links | edit)
- Crandall syndrome (← links | edit)
- Centronuclear myopathy (← links | edit)
- Arts syndrome (← links | edit)
- Hershey bar (← links | edit)
- Lambert Eaton myasthenic syndrome (← links | edit)
- Duncan (← links | edit)
- Alpha-thalassemia x-linked intellectual disability syndrome (← links | edit)
- Cutaneous mastocytoma (← links | edit)
- Monochromacy (← links | edit)
- Nephrogenic diabetes insipidus (← links | edit)
- Lesch Nyhan syndrome (← links | edit)
- McLeod neuroacanthocytosis syndrome (← links | edit)
- Emery–Dreifuss muscular dystrophy (← links | edit)
- Ichthyosis follicularis with alopecia and photophobia syndrome (← links | edit)
- Netherton syndrome (← links | edit)
- Paramyotonia congenita (← links | edit)
- Classical Ehlers-Danlos syndrome (← links | edit)
- Dermatosparaxis Ehlers-Danlos syndrome (← links | edit)
- Cutis laxa, autosomal dominant (← links | edit)
- Renpenning's syndrome (← links | edit)
- Nance–Horan syndrome (← links | edit)
- Immunodysregulation, polyendocrinopathy and enteropathy X-linked (← links | edit)
- Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (← links | edit)
- Deafness hypogonadism syndrome (← links | edit)
- Mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes (← links | edit)
- Orofaciodigital syndrome 9 (← links | edit)
- TARP syndrome (← links | edit)
- Isolated growth hormone deficiency (← links | edit)
- Kallmann syndrome 1 (← links | edit)
- Male pseudohermaphroditism intellectual disability syndrome, Verloes type (← links | edit)
- Myotonic dystrophy type 1 (← links | edit)
- Myotonic dystrophy type 2 (← links | edit)
- Spondyloepiphyseal dysplasia tarda X-linked (← links | edit)
- Congenital pulmonary alveolar proteinosis (← links | edit)
- Immune defect due to absence of thymus (← links | edit)
- Immunodeficiency with hyper IgM type 1 (← links | edit)
- X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia (← links | edit)
- Proud syndrome (← links | edit)
- Anemia sideroblastic and spinocerebellar ataxia (← links | edit)
- Chondrodysplasia punctata 1, X-linked recessive (← links | edit)
- Spondylodysplastic Ehlers-Danlos syndrome (← links | edit)
- Menkes disease (← links | edit)
- Myoclonic epilepsy with ragged red fibers (← links | edit)
- Multiple congenital anomalies-hypotonia-seizures syndrome type 2 (← links | edit)
- Limb-girdle muscular dystrophy type 2I (← links | edit)
- Limb-girdle muscular dystrophy, type 2C (← links | edit)
- Epidermolysa bullosa simplex with muscular dystrophy (← links | edit)
- Araf (← links | edit)
- Glycerol kinase deficiency (← links | edit)
- Limb-girdle muscular dystrophy type 2A (← links | edit)
- Limb-girdle muscular dystrophy type 2B (← links | edit)
- Tubular aggregate myopathy (← links | edit)
- Autosomal dominant centronuclear myopathy (← links | edit)
- Autosomal recessive centronuclear myopathy (← links | edit)
- Bullous dystrophy hereditary macular type (← links | edit)
- Hydrocephalus due to congenital stenosis of aqueduct of sylvius (← links | edit)
- Intellectual disability-developmental delay-contractures syndrome (← links | edit)
- Intermediate congenital nemaline myopathy (← links | edit)
- Isaacs' syndrome (← links | edit)
- Partington syndrome (← links | edit)
- Becker's myotonia (← links | edit)
- Reducing body myopathy (← links | edit)
- Scott Bryant Graham syndrome (← links | edit)
- Spastic paraplegia 2 (← links | edit)
- X-linked intellectual disability, Siderius type (← links | edit)
- X-linked dystonia-parkinsonism/Lubag (← links | edit)
- Van Den Bosch syndrome (← links | edit)
- Arthrochalasia Ehlers-Danlos syndrome (← links | edit)
- Epidermolysis bullosa simplex, Dowling-Meara type (← links | edit)
- Epidermolysis bullosa simplex, generalized (← links | edit)
- Epidermolysis bullosa simplex, localized (← links | edit)
- Epidermolysis bullosa, lethal acantholytic (← links | edit)
- Kyphoscoliotic Ehlers-Danlos syndrome (← links | edit)
- Pretibial epidermolysis bullosa (← links | edit)
- Punctate palmoplantar keratoderma type I (← links | edit)
- Recessive dystrophic epidermolysis bullosa-generalized other (← links | edit)
- Severe generalized recessive dystrophic epidermolysis bullosa (← links | edit)
- Focal palmoplantar and gingival keratosis (← links | edit)
- Conorenal syndrome (← links | edit)
- Hunter syndrome (← links | edit)
- MELAS syndrome (← links | edit)
- Rothmund Thomson syndrome (← links | edit)
- Properdin deficiency (← links | edit)
- Langer–Giedion syndrome (← links | edit)
- Laryngo-onycho-cutaneous syndrome (← links | edit)
- Burnside–Butler syndrome (← links | edit)
- CAPOS syndrome (← links | edit)
- CHAMP1-associated intellectual disability syndrome (← links | edit)
- Camptodactyly-taurinuria syndrome (← links | edit)
- Familial episodic pain syndrome (← links | edit)
- Histidinuria renal tubular defect syndrome (← links | edit)
- Holoprosencephaly-ectrodactyly-cleft lip/palate syndrome (← links | edit)
- LIG4 syndrome (← links | edit)
- Skin fragility-woolly hair-palmoplantar keratoderma syndrome (← links | edit)
- Thickened earlobes-conductive deafness syndrome (← links | edit)
- Thoracic dysplasia-hydrocephalus syndrome (← links | edit)
- Hypohidrotic ectodermal dysplasia with immune deficiency (← links | edit)
- Exner syndrome (← links | edit)
- Otofaciocervical syndrome (← links | edit)
- Smith–Martin–Dodd syndrome (← links | edit)
- Waardenburg anophthalmia syndrome (← links | edit)
- ATR-X syndrome (← links | edit)
- X-linked reticulate pigmentary disorder (← links | edit)
- Hypohidrotic ectodermal dysplasia (← links | edit)
- Megalocornea (← links | edit)
- Familial renal amyloidosis (← links | edit)
- Fructose bisphosphatase deficiency (← links | edit)
- FHL3 (← links | edit)
- FHL1 (← links | edit)
- Retinoschisin (← links | edit)
- XK (protein) (← links | edit)
- Haemo (← links | edit)
- Phosphoglycerate kinase (← links | edit)
- ALD (← links | edit)
- Tranebjaerg–Svejgaard syndrome (← links | edit)
- Kahrizi syndrome (← links | edit)
- Chudley–Lowry–Hoar syndrome (← links | edit)
- Euhidrotic ectodermal dysplasia (← links | edit)
- Inborn urea cycle disorder (← links | edit)
- Van Allen–Myhre syndrome (← links | edit)
- Patterson–Lowry syndrome (← links | edit)
- Partington–Anderson syndrome (← links | edit)
- Bannayan Riley Ruvalcaba syndrome (← links | edit)
- Burnside Butler syndrome (← links | edit)
- XPA (← links | edit)
- Emerin (← links | edit)
- John Menkes (← links | edit)
- Albinism–deafness syndrome (← links | edit)
- Hereditary carrier (← links | edit)
- Sifap (← links | edit)
- Keratosis follicularis-dwarfism-cerebral atrophy syndrome (← links | edit)
- X-linked complicated corpus callosum dysgenesis (← links | edit)
- Morgagni–Stewart–Morel syndrome (← links | edit)
- Template:Congenital malformations and deformations of integument (← links | edit)
- Template:Diseases of myoneural junction and muscle (← links | edit)
- Category:Cutaneous congenital anomalies (← links | edit)
- X-linked sideroblastic anemia and spinocerebellar ataxia (← links | edit)
- Keratosis follicularis-dwarfism-cerebral atrophy syndrome (← links | edit)
- X-linked complicated corpus callosum dysgenesis (← links | edit)
- Template:X-linked disorders (← links | edit)
- Category:X-linked recessive disorders (← links | edit)
