Pages that link to "Mendelian Inheritance in Man"
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The following pages link to Mendelian Inheritance in Man:
Displayed 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Beckwith-Wiedemann syndrome (← links)
- Endometrial stromal sarcoma (← links)
- Cowden syndrome (← links)
- MUTYH polyposis syndrome (← links)
- Fabry disease (← links)
- Xeroderma pigmentosum (← links)
- Steatocystoma (← links)
- Juvenile polyposis syndrome (← links)
- TFEB-rearranged renal cell carcinoma (← links)
- Hereditary hemochromatosis (← links)
- Wilson's disease (← links)
- Nephrotic syndrome (← links)
- NUT carcinoma (← links)
- Parathyroid glands (← links)
- Hereditary hemorrhagic telangiectasia (← links)
- Invasive lobular carcinoma (← links)
- Dysplastic nevus (← links)
- Invasive ductal carcinoma of the pancreas (← links)
- Acute myeloid leukemia (← links)
- McCune-Albright syndrome (← links)
- Urothelial carcinoma (← links)
- Clear cell carcinoma of the ovary (← links)
- Lhermitte-Duclos disease (← links)
- Chondroma (← links)
- Tumour suppressor gene (← links)
- Cystic fibrosis (← links)
- Denys-Drash syndrome (← links)
- Oncogene (← links)
- 22q11.2 deletion syndrome (← links)
- Serous carcinoma of the ovary (← links)
- Behçet's syndrome (← links)
- Prostate cancer (← links)
- Autosomal recessive polycystic kidney disease (← links)
- Adrenoleukodystrophy (← links)
- Bazex syndrome (← links)
- Birt–Hogg–Dubé syndrome (← links)
- Hereditary renal cell carcinoma (← links)
- Ochronosis (← links)
- Paget's disease of the bone (← links)
- Hereditary diffuse gastric cancer (← links)
- KRAS mutation (← links)
- Hereditary breast cancer (← links)
- Transmembrane mucin 1 (← links)
- Hereditary leiomyomatosis and renal cell carcinoma syndrome (← links)
- Cystinosis (← links)
- BRAF V600E mutation (← links)
- Glypican 3 (← links)
- MAP2 (← links)
- GFAP (← links)
- B-cell CLL/lymphoma 2 (← links)