The following pages link to X-linked adrenal hypoplasia congenita
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Sideroblastic anemia (links | edit)
- Dyskeratosis congenita (links | edit)
- Popliteal pterygium syndrome (links | edit)
- Adrenal hypoplasia congenita (redirect page) (links | edit)
- Sex-determination system (links | edit)
- DAX1 (links | edit)
- Glycerol kinase deficiency (links | edit)
- Hyperglycerolemia (links | edit)
- Talk:Adrenal hypoplasia congenita (links | edit)
- User:Roosevelt2015/sandbox (links | edit)
- Misplaced Pages:Version 1.0 Editorial Team/Medical genetics articles by quality log (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Articles (links | edit)
- Congenital adrenal hypoplasia (redirect page) (links | edit)
- Newborn screening (links | edit)
- DAX1 (links | edit)
- Hyperglycerolemia (links | edit)
- Talk:Congenital adrenal hypoplasia (links | edit)
- User:Roosevelt2015/sandbox (links | edit)
- User:Canada Hky/NBS (links | edit)
- Misplaced Pages:Version 1.0 Editorial Team/Medical genetics articles by quality log (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Articles (links | edit)
- X-linked AHC (redirect page) (links | edit)
- Nonsyndromic deafness (links | edit)
- Nephrogenic diabetes insipidus (links | edit)
- Barakat syndrome (links | edit)
- Choroideremia (links | edit)
- Cleidocranial dysostosis (links | edit)
- IPEX syndrome (links | edit)
- Simpson–Golabi–Behmel syndrome (links | edit)
- Hyperimmunoglobulin E syndrome (links | edit)
- X-linked severe combined immunodeficiency (links | edit)
- Primary ovarian insufficiency (links | edit)
- Greig cephalopolysyndactyly syndrome (links | edit)
- Pallister–Hall syndrome (links | edit)
- Centronuclear myopathy (links | edit)
- Léri–Weill dyschondrosteosis (links | edit)
- Oculocerebrorenal syndrome (links | edit)
- ATR-X syndrome (links | edit)
- Holt–Oram syndrome (links | edit)
- Nail–patella syndrome (links | edit)
- Pseudohypoaldosteronism (links | edit)
- Hunter syndrome (links | edit)
- Emery–Dreifuss muscular dystrophy (links | edit)
- McLeod syndrome (links | edit)
- Duane-radial ray syndrome (links | edit)
- Mowat–Wilson syndrome (links | edit)
- Denys–Drash syndrome (links | edit)
- Partial androgen insensitivity syndrome (links | edit)
- X-linked dominant inheritance (links | edit)
- Ectrodactyly–ectodermal dysplasia–cleft syndrome (links | edit)
- X-linked hypophosphatemia (links | edit)
- Lymphedema–distichiasis syndrome (links | edit)
- Hypohidrotic ectodermal dysplasia (links | edit)
- Conradi–Hünermann syndrome (links | edit)
- Hyper-IgM syndrome type 1 (links | edit)
- Axenfeld–Rieger syndrome (links | edit)
- Craniofrontonasal dysplasia (links | edit)
- Papillorenal syndrome (links | edit)
- Campomelic dysplasia (links | edit)
- Properdin deficiency (links | edit)
- Estrogen insensitivity syndrome (links | edit)
- Myotonic dystrophy (links | edit)
- Townes–Brocks syndrome (links | edit)
- Hay–Wells syndrome (links | edit)
- Dent's disease (links | edit)
- Currarino syndrome (links | edit)