Pages that link to "TNFRSF13C"
From WikiMD's Food, Medicine & Wellness Encyclopedia
The following pages link to TNFRSF13C:
Displayed 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- List of OMIM disorder codes (← links | edit)
- Osteopetrosis (← links | edit)
- Donohue syndrome (← links | edit)
- Glanzmann thrombasthenia (← links | edit)
- Laron syndrome (← links | edit)
- Thanatophoric dysplasia (← links | edit)
- Waardenburg syndrome (← links | edit)
- Nevoid basal cell carcinoma syndrome (← links | edit)
- Familial hypercholesterolemia (← links | edit)
- Selective IgA deficiency (← links | edit)
- Gonadotropin-releasing hormone insensitivity (← links | edit)
- Antley–Bixler syndrome (← links | edit)
- Cenani–Lenz syndactylism (← links | edit)
- Follicle-stimulating hormone insensitivity (← links | edit)
- Leukocyte adhesion deficiency-1 (← links | edit)
- Loeys–Dietz syndrome (← links | edit)
- TNF receptor associated periodic syndrome (← links | edit)
- WHIM syndrome (← links | edit)
- Worth syndrome (← links | edit)
- X-linked severe combined immunodeficiency (← links | edit)
- Kallmann syndrome (← links | edit)
- Hereditary hemorrhagic telangiectasia (← links | edit)
- Familial exudative vitreoretinopathy (← links | edit)
- Common variable immunodeficiency (← links | edit)
- Crouzon syndrome (← links | edit)
- Congenital amegakaryocytic thrombocytopenia (← links | edit)
- Congenital insensitivity to pain with anhidrosis (← links | edit)
- Apert syndrome (← links | edit)
- Template:Cell surface receptor deficiencies (← links | edit)
- Gastrointestinal Stromal Tumors (← links | edit)
- Tumor necrosis factor receptor-associated periodic syndrome (← links | edit)
- Template:Clusters of differentiation (← links | edit)
- Nephrogenic diabetes insipidus (← links | edit)
- Complement receptor 1 (← links | edit)
- XX gonadal dysgenesis (← links | edit)
- Worth type autosomal dominant osteosclerosis (← links | edit)
- Juvenile polyposis syndrome (← links | edit)
- Familial hypocalciuric hypercalcemia type 1 (← links | edit)
- Familial hypocalciuric hypercalcemia type 3 (← links | edit)
- Kallmann syndrome 1 (← links | edit)
- Dietz syndrome (← links | edit)
- Pseudohypoparathyroidism type 1A (← links | edit)
- Pseudohypoparathyroidism type 1B (← links | edit)
- Pseudohypoparathyroidism type 2 (← links | edit)
- Leukocyte adhesion deficiency type 1 (← links | edit)
- Achondroplasia (← links | edit)
- Transferrin-crm107 (← links | edit)
- Jansen type metaphyseal chondrodysplasia (← links | edit)
- Osteopetrosis autosomal dominant type 1 (← links | edit)
- Syndactyly Cenani Lenz type (← links | edit)
