Pages that link to "Sjögren–Larsson syndrome"
From WikiMD.com Medical Encyclopedia
The following pages link to Sjögren–Larsson syndrome:
Displayed 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Lymphedema (← links | edit)
- Incontinentia pigmenti (← links | edit)
- List of OMIM disorder codes (← links | edit)
- List of diseases (S) (← links | edit)
- Ichthyosis (← links | edit)
- Bloom syndrome (← links | edit)
- Aplasia cutis congenita (← links | edit)
- Palmoplantar keratoderma (← links | edit)
- Propionic acidemia (← links | edit)
- Inborn errors of metabolism (← links | edit)
- Mastocytosis (← links | edit)
- Miscellaneous (← links | edit)
- Dictionary of neurology (← links | edit)
- Cutis laxa (← links | edit)
- Carnitine-acylcarnitine translocase deficiency (← links | edit)
- Very long-chain acyl-coenzyme A dehydrogenase deficiency (← links | edit)
- Health-encyclopedia-S (← links | edit)
- Diseases-and-disorders-S (← links | edit)
- Template:Congenital malformations and deformations of integument (← links | edit)
- Bloch-sulzberger syndrome (← links | edit)
- Biotinidase deficiency (← links | edit)
- FADH deficiency (redirect page) (← links | edit)
- FALDH deficiency (redirect page) (← links | edit)
- List of rare diseases-F (← links | edit)
- Genetic diseases-F (← links | edit)
- FAO deficiency (redirect page) (← links | edit)
- Fatty aldehyde dehydrogenase deficiency (redirect page) (← links | edit)
- List of rare diseases-F (← links | edit)
- Genetic diseases-F (← links | edit)
- Ichthyosis, spastic neurologic disorder, and oligophrenia (redirect page) (← links | edit)
- Xeroderma pigmentosum (← links | edit)
- Focal dermal hypoplasia (← links | edit)
- Epidermolysis bullosa (← links | edit)
- Epidermolysis bullosa simplex (← links | edit)
- Acute fatty liver of pregnancy (← links | edit)
- Template:Fatty-acid metabolism disorders (← links | edit)
- Myopathic carnitine deficiency (← links | edit)
- Cutaneous mastocytoma (← links | edit)
- Netherton syndrome (← links | edit)
- Classical Ehlers-Danlos syndrome (← links | edit)
- Dermatosparaxis Ehlers-Danlos syndrome (← links | edit)
- Cutis laxa, autosomal dominant (← links | edit)
- Medium-chain acyl-coenzyme A dehydrogenase deficiency (← links | edit)
- Ankyloblepharon-ectodermal defects-cleft lip/palate syndrome (← links | edit)
- 3-alpha hydroxyacyl-CoA dehydrogenase deficiency (← links | edit)
- Carnitine palmitoyl transferase 1A deficiency (← links | edit)
- Spondylodysplastic Ehlers-Danlos syndrome (← links | edit)
- Epidermolysa bullosa simplex with muscular dystrophy (← links | edit)
- 2,4-Dienoyl-CoA reductase deficiency (← links | edit)
- Carnitine palmitoyltransferase 2 deficiency (← links | edit)
- Arthrochalasia Ehlers-Danlos syndrome (← links | edit)
- Epidermolysis bullosa simplex, Dowling-Meara type (← links | edit)
- Epidermolysis bullosa simplex, generalized (← links | edit)
- Epidermolysis bullosa simplex, localized (← links | edit)
