Pages that link to "X-linked dominant inheritance"

The following pages link to X-linked dominant inheritance:

Displaying 27 items.

• Incontinentia pigmenti (← links | edit)
• Genetic disorder (← links | edit)
• Acquired hemophilia A (← links | edit)
• Rett syndrome (← links | edit)
• Dictionary of genetic terms (← links | edit)
• Health topics a-z (← links | edit)
• Lisch epithelial corneal dystrophy (← links | edit)
• Health-encyclopedia-X (← links | edit)
• Bloch-sulzberger syndrome (← links | edit)
• Spinal and bulbar muscular atrophy (← links | edit)
• STAR syndrome (← links | edit)
• Orofaciodigital syndrome 1 (← links | edit)
• Danon disease (← links | edit)
• Centronuclear myopathy (← links | edit)
• Coffin–Lowry syndrome (← links | edit)
• Dictionary-X (← links | edit)
• FMR1 (← links | edit)
• Sigma receptor (← links | edit)
• Conradi–Hünermann syndrome (← links | edit)
• Rett (← links | edit)
• Coffin Lowry syndrome (← links | edit)
• Short-stature homeobox gene (← links | edit)
• X-linked dominance (redirect page) (← links | edit)
  • List of diseases (X) (← links | edit)
• X-linked dominant (redirect page) (← links | edit)
  • Incontinentia pigmenti (← links | edit)
  • Wilms' tumor (← links | edit)
  • Autosomal dominant (← links | edit)
  • Aicardi syndrome (← links | edit)
  • Epstein syndrome (← links | edit)
  • ABCD syndrome (← links | edit)
  • Lisch epithelial corneal dystrophy (← links | edit)
  • X-linked hypophosphatemia (← links | edit)
  • Beta-Propeller Protein-Associated Neurodegeneration (← links | edit)
  • Biemond syndrome (← links | edit)
  • Birk-Barel syndrome (← links | edit)
  • Wildervanck syndrome (← links | edit)
  • STAR syndrome (← links | edit)
  • Stickler syndrome (← links | edit)
  • Orofaciodigital syndrome 1 (← links | edit)
  • Danon disease (← links | edit)
  • Craniofrontonasal dysplasia (← links | edit)
  • Hershey bar (← links | edit)
  • Coffin–Lowry syndrome (← links | edit)
  • Agenesis of the dorsal pancreas (← links | edit)
  • Microphthalmia with linear skin defects syndrome (← links | edit)
  • Bifid nose (← links | edit)
  • Pallister W syndrome (← links | edit)
  • Woods Black Norbury syndrome (← links | edit)
  • 2-methyl-3-hydroxybutyric aciduria (← links | edit)
  • X-linked dominant chondrodysplasia punctata 2 (← links | edit)
  • Brachydactyly Mononen type (← links | edit)
  • Frontometaphyseal dysplasia (← links | edit)
  • Subcortical band heterotopia (← links | edit)
  • Mehes syndrome (← links | edit)
  • X-linked periventricular heterotopia (← links | edit)
  • X-linked intellectual disability, Najm type (← links | edit)
  • Split spinal cord malformation (← links | edit)
  • Focal palmoplantar and gingival keratosis (← links | edit)
  • Conorenal syndrome (← links | edit)
  • X-linked hypertrichosis (← 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)
  • Exner syndrome (← links | edit)
  • Otofaciocervical syndrome (← links | edit)
  • Smith–Martin–Dodd syndrome (← links | edit)
  • Waardenburg anophthalmia syndrome (← links | edit)
  • Familial renal amyloidosis (← links | edit)
  • Fructose bisphosphatase deficiency (← links | edit)
  • PHEX (← links | edit)
  • Marashi–Gorlin syndrome (← links | edit)
  • Familial band heterotopia (← links | edit)
  • OFD syndrome type Figuera (← links | edit)
  • Orofaciodigital syndrome Shashi type (← links | edit)
  • Oral-facial-digital syndrome, type IV (← links | edit)
  • Bannayan Riley Ruvalcaba syndrome (← links | edit)
  • Burnside Butler syndrome (← links | edit)
  • XPA (← links | edit)
  • Hereditary carrier (← links | edit)
  • Mental retardation and microcephaly with pontine and cerebellar hypoplasia (← links | edit)
  • X-linked cone-rod dystrophy, type 1 (← links | edit)
• Mental retardation and microcephaly with pontine and cerebellar hypoplasia (← links | edit)
• Template:X-linked disorders (← links | edit)
• Category:X-linked dominant disorders (← links | edit)