Pages that link to "Mowat–Wilson syndrome"
From WikiMD.com - Food, Medicine & Wellness Encyclopedia
The following pages link to Mowat–Wilson syndrome:
Displayed 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Disease (← links | edit)
- Aldrich syndrome (← links | edit)
- 17-alpha-hydroxylase/17,20 lyase deficiency (← links | edit)
- Androgen insensitivity syndrome (← links | edit)
- Autoimmune polyglandular syndrome type 1 (← links | edit)
- Campomelic dysplasia (← links | edit)
- Chromosome 18q deletion syndrome (← links | edit)
- Congenital nephrotic syndrome (← links | edit)
- Fabry disease (← links | edit)
- Familial hypocalciuric hypercalcemia (← links | edit)
- Myotonic dystrophy (← links | edit)
- Periodic fever syndrome (← links | edit)
- Septo-optic dysplasia (← links | edit)
- Thyroid dyshormonogenesis (← links | edit)
- Waardenburg syndrome (← links | edit)
- X-linked adrenal hypoplasia congenita (← links | edit)
- Pachyonychia congenita (← links | edit)
- Cherubism (← links | edit)
- Miscellaneous (← links | edit)
- Sanfilippo syndrome (← links | edit)
- Lymphedema–distichiasis syndrome (← links | edit)
- Yemenite deaf-blind hypopigmentation syndrome (← links | edit)
- Young–Simpson syndrome (← links | edit)
- Schinzel–Giedion syndrome (← links | edit)
- Camurati–Engelmann disease (← links | edit)
- Follicle-stimulating hormone insensitivity (← links | edit)
- Léri–Weill dyschondrosteosis (← links | edit)
- Loeys–Dietz syndrome (← links | edit)
- Simpson–Golabi–Behmel syndrome (← links | edit)
- Townes–Brocks syndrome (← links | edit)
- Treacher Collins syndrome (← links | edit)
- Yunis–Varon syndrome (← links | edit)
- Health-encyclopedia-M (← links | edit)
- Diseases-and-disorders-M (← links | edit)
- Behr syndrome (← links | edit)
- BRCA1 hereditary breast and ovarian cancer syndrome (← links | edit)
- Brugada syndrome (← links | edit)
- Hirschsprung disease mental retardation syndrome (redirect page) (← links | edit)
- List of rare diseases-H (← links | edit)
- List of syndromes (← links | edit)
- Mental retardation, microcephaly, and distinct facial features with or without Hirschsprung disease (redirect page) (← links | edit)
- Spinal and bulbar muscular atrophy (← links | edit)
- Meesmann corneal dystrophy (← links | edit)
- Dentinogenesis imperfecta (← links | edit)
- Caspase-8 deficiency (← links | edit)
- Alveolar capillary dysplasia (← links | edit)
- Template:Transcription factor and coregulator deficiencies (← links | edit)
- Leri Weill dyschondrosteosis (← links | edit)
- Hypotrichosis–lymphedema–telangiectasia syndrome (← links | edit)
- Axenfeld–Rieger syndrome (← links | edit)
- Cartilage–hair hypoplasia (← links | edit)
- Congenital adrenal hyperplasia due to 17α-hydroxylase deficiency (← links | edit)
