Pages that link to "Online Mendelian Inheritance in Man"
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The following pages link to Online Mendelian Inheritance in Man:
Displayed 50 items.
- Familial male precocious puberty (← links)
- Fountain syndrome (← links)
- Glucocorticoid deficiency 1 (← links)
- Hypertrichosis lanuginosa (← links)
- Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase deficiency (← links)
- Methylmalonic acidemia (← links)
- Pacman dysplasia (← links)
- Zaspopathy (← links)
- Hereditary spherocytosis (← links)
- Congenital absence of the vas deferens (← links)
- Zori Stalker Williams syndrome (← links)
- Freeman-Sheldon syndrome (← links)
- Hyperammonemia (← links)
- Spermatogenesis arrest (← links)
- ICF syndrome (← links)
- Meleda Disease (← links)
- Michelin tire baby syndrome (← links)
- Mullerian agenesis (← links)
- Pachygyria (← links)
- Pentalogy of Cantrell (← links)
- Progressive supranuclear palsy (← links)
- Mevalonic aciduria (← links)
- Methylmalonyl-CoA mutase deficiency (← links)
- Neuronal ceroid lipofuscinosis (← links)
- HEC syndrome (← links)
- Biomolecular Object Network Databank (← links)
- Donohue syndrome (← links)
- Monosomy 9p (← links)
- Nezelof syndrome (← links)
- Grey platelet syndrome (← links)
- Patterson syndrome (← links)
- Da Costa's syndrome (← links)
- Hyper IgM Syndrome Type 2 (← links)
- Regulatory T cell (← links)
- Melanocortin 1 receptor (← links)
- CD244 (← links)
- Phosphoinositide 3-kinase (← links)
- C-Raf (← links)
- Neuregulin (← links)
- Hedgehog signaling pathway (← links)
- H19 (gene) (← links)
- Branchio-oto-renal syndrome (← links)
- PACS1 (← links)
- CCNB1IP1 (← links)
- TFAP2A (← links)
- RIPK1 (← links)
- Sequestosome 1 (← links)
- Interferon gamma receptor 1 (← links)
- NT5E (← links)
- SAT1 (gene) (← links)