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309801
MCOPS7
MICROPHTHALMIA, SYNDROMIC 7
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Neoplasms
Cysts
Neoplasms by Histologic Type
Neoplasms, Connective and Soft Tissue
Neoplasms, Connective Tissue
Neoplasms, Fibrous Tissue
Fibroma
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dysostoses
Focal Dermal Hypoplasia
Synostosis
Craniosynostoses
Syndactyly
Foot Deformities
Foot Deformities, Congenital
Hand Deformities
Hand Deformities, Congenital
Jaw Diseases
Jaw Abnormalities
Cleft Palate
Muscular Diseases
Muscle Weakness
Paralyses, Familial Periodic
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniosynostoses
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Microcephaly
Plagiocephaly
Craniosynostoses
Limb Deformities, Congenital
Lower Extremity Deformities, Congenital
Foot Deformities, Congenital
Polydactyly
Syndactyly
Upper Extremity Deformities, Congenital
Hand Deformities, Congenital
Synostosis
Craniosynostoses
Syndactyly
Digestive System Diseases
Digestive System Fistula
Intestinal Fistula
Rectal Fistula
Gastrointestinal Diseases
Intestinal Diseases
Intestinal Fistula
Rectal Fistula
Rectal Diseases
Rectal Fistula
Stomatognathic Diseases
Jaw Diseases
Jaw Abnormalities
Cleft Palate
Mouth Diseases
Mouth Abnormalities
Cleft Palate
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Mouth Abnormalities
Cleft Palate
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Basal Ganglia Diseases
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Weakness
Neuromuscular Diseases
Muscular Diseases
Paralyses, Familial Periodic
Neuromuscular Junction Diseases
Myasthenic Syndromes, Congenital
Eye Diseases
Corneal Diseases
Corneal Opacity
Eye Abnormalities
Anophthalmos
Microphthalmos
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Retinitis Pigmentosa
Lens Diseases
Cataract
Retinal Diseases
Retinal Degeneration
Retinal Dystrophies
Retinitis Pigmentosa
Scleral Diseases
Male Urogenital Diseases
Genital Diseases, Male
Penile Diseases
Hypospadias
Urogenital Abnormalities
Disorders of Sex Development
46, XX Disorders of Sex Development
Gonadal Dysgenesis, 46,XX
46, XY Disorders of Sex Development
Gonadal Dysgenesis, 46,XY
Gonadal Dysgenesis
Gonadal Dysgenesis, 46,XX
Gonadal Dysgenesis, 46,XY
Hypospadias
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urogenital Abnormalities
Disorders of Sex Development
46, XX Disorders of Sex Development
Gonadal Dysgenesis, 46,XX
46, XY Disorders of Sex Development
Gonadal Dysgenesis, 46,XY
Gonadal Dysgenesis
Gonadal Dysgenesis, 46,XX
Gonadal Dysgenesis, 46,XY
Hypospadias
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Heart Diseases
Arrhythmias, Cardiac
Tachycardia
Tachycardia, Ventricular
Cardiomyopathies
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Ectodermal Dysplasia
Focal Dermal Hypoplasia
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Chromosome Disorders
Eye Abnormalities
Anophthalmos
Microphthalmos
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Craniosynostoses
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Microcephaly
Plagiocephaly
Craniosynostoses
Limb Deformities, Congenital
Foot Deformities, Congenital
Hand Deformities, Congenital
Polydactyly
Syndactyly
Synostosis
Craniosynostoses
Syndactyly
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Skin Abnormalities
Ectodermal Dysplasia
Focal Dermal Hypoplasia
Stomatognathic System Abnormalities
Maxillofacial Abnormalities
Jaw Abnormalities
Cleft Palate
Mouth Abnormalities
Cleft Palate
Urogenital Abnormalities
Disorders of Sex Development
46, XX Disorders of Sex Development
Gonadal Dysgenesis, 46,XX
46, XY Disorders of Sex Development
Gonadal Dysgenesis, 46,XY
Gonadal Dysgenesis
Gonadal Dysgenesis, 46,XX
Gonadal Dysgenesis, 46,XY
Hypospadias
Genetic Diseases, Inborn
Chromosome Disorders
Eye Diseases, Hereditary
Albinism
Albinism, Ocular
Retinitis Pigmentosa
Genetic Diseases, X-Linked
Focal Dermal Hypoplasia
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Ocular
Metal Metabolism, Inborn Errors
Paralyses, Familial Periodic
Myasthenic Syndromes, Congenital
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Ectodermal Dysplasia
Focal Dermal Hypoplasia
Infant, Newborn, Diseases
Infant, Premature, Diseases
Skin and Connective Tissue Diseases
Skin Diseases
Erythema
Pigmentation Disorders
Hypopigmentation
Albinism
Albinism, Ocular
Skin Abnormalities
Ectodermal Dysplasia
Focal Dermal Hypoplasia
Skin Diseases, Genetic
Albinism
Albinism, Ocular
Ectodermal Dysplasia
Focal Dermal Hypoplasia
Nutritional and Metabolic Diseases
Metabolic Diseases
Calcium Metabolism Disorders
Calcinosis
Metabolism, Inborn Errors
Amino Acid Metabolism, Inborn Errors
Albinism
Albinism, Ocular
Metal Metabolism, Inborn Errors
Paralyses, Familial Periodic
Endocrine System Diseases
Gonadal Disorders
Disorders of Sex Development
46, XX Disorders of Sex Development
Gonadal Dysgenesis, 46,XX
46, XY Disorders of Sex Development
Gonadal Dysgenesis, 46,XY
Gonadal Dysgenesis
Gonadal Dysgenesis, 46,XX
Gonadal Dysgenesis, 46,XY
Animal Diseases
Disease Models, Animal
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Cysts
Fistula
Digestive System Fistula
Intestinal Fistula
Rectal Fistula
Pathologic Processes
Arrhythmias, Cardiac
Tachycardia
Tachycardia, Ventricular
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Sex Chromosome Aberrations
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Chronic Disease
Diseases in Twins
Recurrence
Muscle Weakness
Signs and Symptoms
Neurologic Manifestations
Neuromuscular Manifestations
Muscle Weakness
Database Center for Life Science
