Home > D. General pathology > Genetic and developmental anomalies > Cousin syndrome
Cousin syndrome
MIM.260660
Monday 4 May 2009
Cousin syndrome is caused by mutation in the TBX15 gene (MIM.604127).
D. General pathology
- Ageing
- Blood and immunity
- Endocrine systemic anomalies
- Environmental and occupational diseases
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Genetic and developmental anomalies
- Genetic metabolic diseases
- Chromosomal diseases
- Malformative associations
- Infectious diseases
- Nutritional diseases
- Therapy, Toxics and drugs
- Vascular pathology
