Pages that link to "PTCH1"
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- Genetic disorder (links | edit)
- Oncogene (links | edit)
- P53 (links | edit)
- Tumor suppressor gene (links | edit)
- Achondroplasia (links | edit)
- Skin cancer (links | edit)
- Cenani–Lenz syndactylism (links | edit)
- Hirschsprung's disease (links | edit)
- Congenital hypothyroidism (links | edit)
- Sonic hedgehog protein (links | edit)
- Ras GTPase (links | edit)
- BRCA1 (links | edit)
- Osteopetrosis (links | edit)
- Gastrointestinal stromal tumor (links | edit)
- Bcl-2 (links | edit)
- Waardenburg syndrome (links | edit)
- Basal-cell carcinoma (links | edit)
- Hereditary hemorrhagic telangiectasia (links | edit)
- Glanzmann's thrombasthenia (links | edit)
- Persistent Müllerian duct syndrome (links | edit)
- Platelet-derived growth factor (links | edit)
- Kallmann syndrome (links | edit)
- Congenital insensitivity to pain with anhidrosis (links | edit)
- BRCA2 (links | edit)
- SDHD (links | edit)
- Crouzon syndrome (links | edit)
- Aspirin-exacerbated respiratory disease (links | edit)
- Microphthalmia (links | edit)
- Apert syndrome (links | edit)
- Thanatophoric dysplasia (links | edit)
- Morphogen (links | edit)
- Protein kinase B (links | edit)
- Epidermal growth factor receptor (links | edit)
- P73 (links | edit)
- Leber congenital amaurosis (links | edit)
- Hypogammaglobulinemia (links | edit)
- Hepatocyte growth factor receptor (links | edit)
- Hypochondroplasia (links | edit)
- HER2 (links | edit)
- Common variable immunodeficiency (links | edit)
- ABCD syndrome (links | edit)
- Stathmin (links | edit)
- PTEN (gene) (links | edit)
- Chromosome 9 (links | edit)
- Jackson–Weiss syndrome (links | edit)
- Pfeiffer syndrome (links | edit)
- Nephrogenic diabetes insipidus (links | edit)
- Pseudohypoparathyroidism (links | edit)
- Adenomatous polyposis coli (links | edit)
- HRAS (links | edit)