MeSH Treeview
Query OMIM entry list
108300
STL1
STICKLER SYNDROME, TYPE I
→
High-scoring List
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Osteochondrodysplasias
Jaw Diseases
Jaw Abnormalities
Cleft Palate
Micrognathism
Pierre Robin Syndrome
Maxillary Diseases
Joint Diseases
Arthritis
Joint Instability
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Micrognathism
Pierre Robin Syndrome
Stomatognathic Diseases
Jaw Diseases
Jaw Abnormalities
Cleft Palate
Micrognathism
Pierre Robin Syndrome
Maxillary Diseases
Mouth Diseases
Lip Diseases
Cleft Lip
Mouth Abnormalities
Cleft Lip
Cleft Palate
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Micrognathism
Pierre Robin Syndrome
Mouth Abnormalities
Cleft Lip
Cleft Palate
Tooth Abnormalities
Anodontia
Tooth Diseases
Malocclusion
Tooth Abnormalities
Anodontia
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Nervous System Diseases
Cranial Nerve Diseases
Ocular Motility Disorders
Strabismus
Esotropia
Neurologic Manifestations
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Vision Disorders
Blindness
Eye Diseases
Corneal Diseases
Keratitis
Eye Abnormalities
Eye Diseases, Hereditary
Lens Diseases
Aphakia
Cataract
Ocular Hypertension
Glaucoma
Ocular Motility Disorders
Strabismus
Esotropia
Refractive Errors
Myopia
Retinal Diseases
Retinal Degeneration
Retinal Detachment
Uveal Diseases
Uveitis
Vision Disorders
Blindness
Night Blindness
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Cardiovascular Diseases
Heart Diseases
Heart Valve Diseases
Heart Valve Prolapse
Mitral Valve Prolapse
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Eye Abnormalities
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Micrognathism
Pierre Robin Syndrome
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Micrognathism
Pierre Robin Syndrome
Mouth Abnormalities
Cleft Lip
Cleft Palate
Tooth Abnormalities
Anodontia
Genetic Diseases, Inborn
Chromosome Disorders
Dwarfism
Eye Diseases, Hereditary
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Lysosomal Storage Diseases
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Collagen Diseases
Mucinoses
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Lysosomal Storage Diseases
Mucopolysaccharidoses
Mucopolysaccharidosis IV
Endocrine System Diseases
Dwarfism
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Disease Progression
Facies
Signs and Symptoms
Neurologic Manifestations
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Hearing Loss, Sensorineural
Vision Disorders
Blindness
Database Center for Life Science
