Pages that link to "Waardenburg syndrome"
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The following pages link to Waardenburg syndrome:
Displayed 95 items.
- Tyrosinemia (← links)
- Pallor (← links)
- Hypomelanosis (← links)
- Trimethylaminuria (← links)
- Wardenberg syndrome (redirect page) (← links)
- The genetic basis of heart disease (← links)
- Genetic Disorders (← links)
- Chromosome 22 (← links)
- List of diseases (W) (← links)
- List of genetic disorders (← links)
- Iris (anatomy) (← links)
- Canthus (anatomy) (← links)
- Eye color (← links)
- Heterochromia (← links)
- Endothelin receptor (← links)
- Chromosome 2 (human) (← links)
- Chromosome 3 (human) (← links)
- Chromosome 22 (human) (← links)
- Chromosome 20 (human) (← links)
- Chromosome 8 (human) (← links)
- Chromosome 13 (human) (← links)
- Glutathione synthetase deficiency (← links)
- Guanidinoacetate methyltransferase deficiency (← links)
- Hyperlysinemia (← links)
- Hypermethioninemia (← links)
- Hyperprolinemia (← links)
- Isobutyryl-coenzyme A dehydrogenase deficiency (← links)
- Microphthalmia (← links)
- Ornithine translocase deficiency (← links)
- Prolidase deficiency (← links)
- Sarcosinemia (← links)
- Succinic semialdehyde dehydrogenase deficiency (← links)
- Urea cycle disorder (← links)
- Pax genes (← links)
- PAX3 (← links)
- Microphthalmia-associated transcription factor (← links)
- List of geneticists (← links)
- Inborn error of metabolism (← links)
- Testpage3 (← links)
- Waardenburg syndrome type 1 (redirect page) (← links)
- Waardenburg syndrome type 2 (redirect page) (← links)
- Waardenburg syndrome type 2A (redirect page) (← links)
- Waardenburg syndrome type 2B (redirect page) (← links)
- Waardenburg syndrome type 3 (redirect page) (← links)
- Waardenburg syndrome, type 4 (redirect page) (← links)
- Waardenburg type Pierpont (redirect page) (← links)
- Methylmalonyl-CoA mutase deficiency (← links)
- List of ICD-9 codes 240-279: Endocrine, nutritional and metabolic diseases, and immunity disorders (← links)
- Hypertelorism (← links)
- Chromosome 2 (← links)
- Chromosome 3 (← links)
- Chromosome 13 (← links)
- Chromosome 8 (← links)
- Glossary of medical terms related to communications disorders (← links)
- Endothelin 3 (← links)
- SOX10 (← links)
- Wardenberg's Syndrome (redirect page) (← links)
- Wardenberg's syndrome (redirect page) (← links)
- Waardenburg's syndrome (redirect page) (← links)
- Inborn errors of renal tubular transport (← links)
- Ferret (← links)
- Hypervalinemia (← links)
- Organic acidemia (← links)
- Carnosinemia (← links)
- Hawkinsinuria (← links)
- Inborn errors of amino acid metabolism (← links)
- D-Glyceric acidemia (← links)
- Urocanic aciduria (← links)
- Amino acid transport disorder (← links)
- Argininemia (← links)
- 2-Hydroxyglutaric aciduria (← links)
- Type I tyrosinemia (← links)
- Type II tyrosinemia (← links)
- Type III tyrosinemia (← links)
- Klein-Waardenburg syndrome (redirect page) (← links)
- Waardenburg-Klein syndrome (redirect page) (← links)
- Mende's syndrome II (redirect page) (← links)
- Van der Hoeve-Halbertsma-Waardenburg syndrome (redirect page) (← links)
- Ptosis-Epicanthus syndrome (redirect page) (← links)
- Van der Hoeve-Halbertsma-Gualdi syndrome (redirect page) (← links)
- Waardenburg Syndrome (redirect page) (← links)
- ABCD syndrome (← links)
- Albinism (patient information) (← links)
- Albinism overview (← links)
- Albinism differential diagnosis (← links)
- Hearing impairment pathophysiology (← links)
- Deafness causes (← links)
- Poliosis (← links)
- 2-methylbutyryl-coenzyme a dehydrogenase deficiency (← links)
- Hypertryptophanemia (← links)
- Differentiating Albinism from other diseases (← links)
- WS2B (← links)
- Endothelin B receptor (← links)
- Chromosome 20 (← links)
- Enhancer box gene transcriptions (← links)
- Template:Amino acid metabolic pathology (← links)