The following pages link to Low-density lipoprotein receptor-related protein 4
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View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- High-density lipoprotein (links | edit)
- Lipid (links | edit)
- Myasthenia gravis (links | edit)
- Low-density lipoprotein (links | edit)
- Triglyceride (links | edit)
- Lipoprotein (links | edit)
- Very low-density lipoprotein (links | edit)
- Chylomicron (links | edit)
- Intermediate-density lipoprotein (links | edit)
- Lipoprotein lipase (links | edit)
- Apolipoprotein (links | edit)
- LDL receptor (links | edit)
- Cholesteryl ester transfer protein (links | edit)
- Apolipoprotein E (links | edit)
- Apolipoprotein B (links | edit)
- Apolipoprotein C-II (links | edit)
- Apolipoprotein C-I (links | edit)
- Lecithin–cholesterol acyltransferase (links | edit)
- Lipoprotein(a) (links | edit)
- LDL-receptor-related protein-associated protein (links | edit)
- Apolipoprotein AI (links | edit)
- Apolipoprotein C-III (links | edit)
- Apolipoprotein C-IV (links | edit)
- Apolipoprotein D (links | edit)
- Apolipoprotein H (links | edit)
- Low-density lipoprotein receptor-related protein 8 (links | edit)
- Hepatic lipase (links | edit)
- ABCA1 (links | edit)
- APOA5 (links | edit)
- Apolipoprotein A-II (links | edit)
- APOA4 (links | edit)
- Phospholipid transfer protein (links | edit)
- LRP2 (links | edit)
- LRP1 (links | edit)
- LRP5 (links | edit)
- Microsomal triglyceride transfer protein (links | edit)
- LRP6 (links | edit)
- ABCG5 (links | edit)
- ABCG8 (links | edit)
- LRP1B (links | edit)
- LRP10 (links | edit)
- Lipoprotein receptor-related protein (links | edit)
- Apolipoprotein C (links | edit)
- Apolipoprotein L (links | edit)
- LRP3 (links | edit)
- Lipidology (links | edit)
- LRP4 (gene) (redirect page) (links | edit)
- Low density lipoprotein receptor-related protein 4 (redirect page) (links | edit)
- Genetic disorder (links | edit)
- Achondroplasia (links | edit)
- Cenani–Lenz syndactylism (links | edit)
- Hirschsprung's disease (links | edit)
- Congenital hypothyroidism (links | edit)
- Osteopetrosis (links | edit)
- Gastrointestinal stromal tumor (links | edit)
- Waardenburg syndrome (links | edit)
- Hereditary hemorrhagic telangiectasia (links | edit)
- Glanzmann's thrombasthenia (links | edit)
- Persistent Müllerian duct syndrome (links | edit)
- Kallmann syndrome (links | edit)
- Congenital insensitivity to pain with anhidrosis (links | edit)
- Crouzon syndrome (links | edit)
- Aspirin-exacerbated respiratory disease (links | edit)
- Apert syndrome (links | edit)
- Thanatophoric dysplasia (links | edit)
- Leber congenital amaurosis (links | edit)
- Hypogammaglobulinemia (links | edit)
- Hypochondroplasia (links | edit)
- Common variable immunodeficiency (links | edit)
- ABCD syndrome (links | edit)
- Jackson–Weiss syndrome (links | edit)
- Pfeiffer syndrome (links | edit)
- Nephrogenic diabetes insipidus (links | edit)
- Pseudohypoparathyroidism (links | edit)
- Familial male-limited precocious puberty (links | edit)
- X-linked severe combined immunodeficiency (links | edit)
- Selective immunoglobulin A deficiency (links | edit)
- Nevoid basal-cell carcinoma syndrome (links | edit)
- Piebaldism (links | edit)
- Robinow syndrome (links | edit)
- Low-density lipoprotein receptor gene family (links | edit)
- XX gonadal dysgenesis (links | edit)
- TNF receptor associated periodic syndrome (links | edit)
- Loeys–Dietz syndrome (links | edit)
- Hypohidrotic ectodermal dysplasia (links | edit)
- Familial hypercholesterolemia (links | edit)
- Jansen's metaphyseal chondrodysplasia (links | edit)
- Juvenile polyposis syndrome (links | edit)
- Laron syndrome (links | edit)
- Muenke syndrome (links | edit)
- Rabson–Mendenhall syndrome (links | edit)
- WHIM syndrome (links | edit)
- Antley–Bixler syndrome (links | edit)
- LRP4 (links | edit)
- Congenital amegakaryocytic thrombocytopenia (links | edit)
- Worth syndrome (links | edit)
- Familial hypocalciuric hypercalcemia (links | edit)
- Leukocyte adhesion deficiency-1 (links | edit)
- Surfactant metabolism dysfunction (links | edit)
- Achondroplasia in children (links | edit)
- List of OMIM disorder codes (links | edit)
- Donnai–Barrow syndrome (links | edit)
- Familial exudative vitreoretinopathy (links | edit)
- Donohue syndrome (links | edit)
- Leydig cell hypoplasia (links | edit)
- Gonadotropin-releasing hormone insensitivity (links | edit)
- Follicle-stimulating hormone insensitivity (links | edit)
- SNED1 (links | edit)
- Gonadotropin insensitivity (links | edit)
- User:AleLopez14/sandbox (links | edit)
- User:Gibso.danny/sandbox (links | edit)
- User:Janeannyoung/sandbox (links | edit)
- User:Pdesai93/sandbox (links | edit)
- User:Egeorge01/sandbox (links | edit)
- User:Isaacadu1/sandbox (links | edit)
- User:Dmil3422/Laron Syndrome (links | edit)
- Template:Cell surface receptor deficiencies (links | edit)
- Remnant cholesterol (links | edit)
- Transient neonatal myasthenia gravis (links | edit)