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Query OMIM entry list
145701
HTC1
HYPERTRICHOSIS UNIVERSALIS CONGENITA, AMBRAS TYPE
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Stomatognathic Diseases
Mouth Diseases
Periodontal Diseases
Gingival Diseases
Gingival Overgrowth
Gingival Hyperplasia
Stomatognathic System Abnormalities
Tooth Abnormalities
Tooth Diseases
Tooth Abnormalities
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Stomatognathic System Abnormalities
Tooth Abnormalities
Genetic Diseases, Inborn
Chromosome Disorders
Skin and Connective Tissue Diseases
Skin Diseases
Hair Diseases
Hypertrichosis
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Facial Asymmetry
Pathologic Processes
Chromosome Aberrations
Chromosome Breakage
Chromosome Inversion
Disease
Syndrome
Database Center for Life Science
