MeSH Treeview
Query OMIM entry list
300276
-
ECTODYSPLASIN RECEPTOR, X-LINKED
→
High-scoring List
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Ectodermal Dysplasia
Skin Abnormalities
Ectodermal Dysplasia
Genetic Diseases, Inborn
Skin Diseases, Genetic
Ectodermal Dysplasia
Skin and Connective Tissue Diseases
Skin Diseases
Skin Abnormalities
Ectodermal Dysplasia
Skin Diseases, Genetic
Ectodermal Dysplasia
Database Center for Life Science