MeSH Treeview
Query OMIM entry list
206900
MCOPS3
MICROPHTHALMIA, SYNDROMIC 3
→
High-scoring List
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Synostosis
Craniosynostoses
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniosynostoses
Plagiocephaly
Craniosynostoses
Synostosis
Craniosynostoses
Digestive System Diseases
Digestive System Abnormalities
Esophageal Atresia
Digestive System Fistula
Esophageal Fistula
Tracheoesophageal Fistula
Gastrointestinal Diseases
Esophageal Diseases
Esophageal Atresia
Esophageal Fistula
Tracheoesophageal Fistula
Respiratory Tract Diseases
Respiratory Tract Fistula
Tracheoesophageal Fistula
Tracheal Diseases
Tracheoesophageal Fistula
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Nervous System Diseases
Neurologic Manifestations
Neurobehavioral Manifestations
Psychomotor Disorders
Sensation Disorders
Hearing Disorders
Eye Diseases
Eye Abnormalities
Anophthalmos
Microphthalmos
Eye Diseases, Hereditary
Retinitis Pigmentosa
Lens Diseases
Cataract
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Scleral Diseases
Male Urogenital Diseases
Genital Diseases, Male
Penile Diseases
Hypospadias
Testicular Diseases
Cryptorchidism
Urogenital Abnormalities
Cryptorchidism
Hypospadias
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urogenital Abnormalities
Hypospadias
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Digestive System Abnormalities
Esophageal Atresia
Eye Abnormalities
Anophthalmos
Microphthalmos
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniosynostoses
Plagiocephaly
Craniosynostoses
Synostosis
Craniosynostoses
Urogenital Abnormalities
Cryptorchidism
Hypospadias
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Retinitis Pigmentosa
Infant, Newborn, Diseases
Infant, Premature, Diseases
Endocrine System Diseases
Gonadal Disorders
Testicular Diseases
Cryptorchidism
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Fistula
Digestive System Fistula
Esophageal Fistula
Tracheoesophageal Fistula
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Diseases in Twins
Facies
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Psychomotor Disorders
Sensation Disorders
Hearing Disorders
Database Center for Life Science
