MeSH Treeview
Query OMIM entry list
302803
-
CHARCOT-MARIE-TOOTH PERONEAL MUSCULAR ATROPHY, X-LINKED, WITH APLASIA CUTIS CONGENITA
→
High-scoring List
Nervous System Diseases
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Neuromuscular Diseases
Peripheral Nervous System Diseases
Polyneuropathies
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Ectodermal Dysplasia
Nervous System Malformations
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
Skin Abnormalities
Ectodermal Dysplasia
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
Hereditary Sensory and Motor Neuropathy
Charcot-Marie-Tooth Disease
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
