MeSH Treeview
Query OMIM entry list
180500
RIEG1
RIEGER SYNDROME, TYPE 1
→
High-scoring List
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Craniofacial Dysostosis
Jaw Diseases
Jaw Abnormalities
Prognathism
Mandibular Diseases
Prognathism
Joint Diseases
Hip Dislocation, Congenital
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Maxillofacial Abnormalities
Jaw Abnormalities
Prognathism
Hip Dislocation, Congenital
Limb Deformities, Congenital
Digestive System Diseases
Gastrointestinal Diseases
Intestinal Diseases
Rectal Diseases
Stomatognathic Diseases
Jaw Diseases
Jaw Abnormalities
Prognathism
Mandibular Diseases
Prognathism
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Prognathism
Tooth Abnormalities
Anodontia
Dental Enamel Hypoplasia
Tooth Diseases
Malocclusion
Malocclusion, Angle Class II
Tooth Abnormalities
Anodontia
Dental Enamel Hypoplasia
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Hypothalamic Diseases
Pituitary Diseases
Hypopituitarism
Cranial Nerve Diseases
Ocular Motility Disorders
Strabismus
Exotropia
Nervous System Malformations
Neural Tube Defects
Anencephaly
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Sensation Disorders
Hearing Disorders
Vision Disorders
Color Vision Defects
Eye Diseases
Eye Abnormalities
Coloboma
Microphthalmos
Ocular Hypertension
Glaucoma
Ocular Motility Disorders
Strabismus
Exotropia
Uveal Diseases
Iris Diseases
Vision Disorders
Color Vision Defects
Male Urogenital Diseases
Genital Diseases, Male
Penile Diseases
Hypospadias
Urogenital Abnormalities
Hypospadias
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urogenital Abnormalities
Hypospadias
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Abnormalities, Severe Teratoid
Anencephaly
Chromosome Disorders
Eye Abnormalities
Coloboma
Microphthalmos
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniofacial Dysostosis
Maxillofacial Abnormalities
Jaw Abnormalities
Prognathism
Hip Dislocation, Congenital
Limb Deformities, Congenital
Nervous System Malformations
Neural Tube Defects
Anencephaly
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Prognathism
Tooth Abnormalities
Anodontia
Dental Enamel Hypoplasia
Urogenital Abnormalities
Hypospadias
Genetic Diseases, Inborn
Chromosome Disorders
Infant, Newborn, Diseases
Hernia, Umbilical
Nutritional and Metabolic Diseases
Nutrition Disorders
Malnutrition
Deficiency Diseases
Endocrine System Diseases
Gonadal Disorders
Hypogonadism
Eunuchism
Pituitary Diseases
Hypopituitarism
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hernia
Hernia, Abdominal
Hernia, Ventral
Hernia, Umbilical
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Translocation, Genetic
Disease
Syndrome
Growth Disorders
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Psychomotor Disorders
Sensation Disorders
Hearing Disorders
Vision Disorders
Color Vision Defects
Database Center for Life Science