The following pages link to Coffin–Lowry syndrome
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Carpenter syndrome (links | edit)
- Metachondromatosis (links | edit)
- Dyskeratosis congenita (links | edit)
- McCune–Albright syndrome (links | edit)
- X-linked adrenal hypoplasia congenita (links | edit)
- Nephrogenic diabetes insipidus (links | edit)
- Costello syndrome (links | edit)
- ZAP70 deficiency (links | edit)
- Choroideremia (links | edit)
- Carney complex (links | edit)
- Bannayan–Riley–Ruvalcaba syndrome (links | edit)
- IPEX syndrome (links | edit)
- Simpson–Golabi–Behmel syndrome (links | edit)
- X-linked severe combined immunodeficiency (links | edit)
- Seckel syndrome (links | edit)
- Centronuclear myopathy (links | edit)
- Coffin-lowry syndrome (redirect page) (links | edit)
- List of MeSH codes (C16) (links | edit)
- Oculocerebrorenal syndrome (links | edit)
- ATR-X syndrome (links | edit)
- Pseudohypoaldosteronism (links | edit)
- Hunter syndrome (links | edit)
- Emery–Dreifuss muscular dystrophy (links | edit)
- McLeod syndrome (links | edit)
- Pseudopseudohypoparathyroidism (links | edit)
- Partial androgen insensitivity syndrome (links | edit)
- Noonan syndrome with multiple lentigines (links | edit)
- X-linked dominant inheritance (links | edit)
- X-linked hypophosphatemia (links | edit)
- Hypohidrotic ectodermal dysplasia (links | edit)
- Conradi–Hünermann syndrome (links | edit)
- Hyper-IgM syndrome type 1 (links | edit)
- Craniofrontonasal dysplasia (links | edit)
- Aarskog–Scott syndrome (links | edit)
- Properdin deficiency (links | edit)
- Myotonic dystrophy (links | edit)
- Polycystic liver disease (links | edit)
- Juvenile primary lateral sclerosis (links | edit)
- Dent's disease (links | edit)
- Oguchi disease (links | edit)
- Ribosomal s6 kinase (links | edit)
- Bone disease (links | edit)
- Brunner syndrome (links | edit)
- RPS6KA3 (links | edit)
- Lhermitte–Duclos disease (links | edit)
- X-linked lymphoproliferative disease (links | edit)
- Chylomicron retention disease (links | edit)
- Ocular albinism (links | edit)
- Orofaciodigital syndrome 1 (links | edit)
- Focal dermal hypoplasia (links | edit)