MeSH Treeview
Query OMIM entry list
208155
-
ARTHROGRYPOSIS MULTIPLEX CONGENITA WITH WHISTLING FACE
→
High-scoring List
Musculoskeletal Diseases
Jaw Diseases
Jaw Abnormalities
Pierre Robin Syndrome
Joint Diseases
Arthrogryposis
Muscular Diseases
Arthrogryposis
Musculoskeletal Abnormalities
Arthrogryposis
Craniofacial Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Pierre Robin Syndrome
Stomatognathic Diseases
Jaw Diseases
Jaw Abnormalities
Pierre Robin Syndrome
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Pierre Robin Syndrome
Nervous System Diseases
Central Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Musculoskeletal Abnormalities
Arthrogryposis
Craniofacial Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Pierre Robin Syndrome
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Pierre Robin Syndrome
Nutritional and Metabolic Diseases
Metabolic Diseases
Calcium Metabolism Disorders
Calcinosis
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Database Center for Life Science
