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309580
MRXHF1
MENTAL RETARDATION-HYPOTONIC FACIES SYNDROME, X-LINKED, 1
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Foot Deformities
Foot Deformities, Congenital
Clubfoot
Hand Deformities
Hand Deformities, Congenital
Muscular Diseases
Muscle Spasticity
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Limb Deformities, Congenital
Lower Extremity Deformities, Congenital
Foot Deformities, Congenital
Clubfoot
Upper Extremity Deformities, Congenital
Hand Deformities, Congenital
Otorhinolaryngologic Diseases
Ear Diseases
Hearing Disorders
Hearing Loss
Deafness
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Seizures
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Intellectual Disability
Mental Retardation, X-Linked
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Spasticity
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
Eye Diseases
Eye Abnormalities
Male Urogenital Diseases
Genital Diseases, Male
Testicular Diseases
Cryptorchidism
Urogenital Abnormalities
Cryptorchidism
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urogenital Abnormalities
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Hemolytic
Anemia, Hemolytic, Congenital
Thalassemia
alpha-Thalassemia
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Eye Abnormalities
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Limb Deformities, Congenital
Foot Deformities, Congenital
Clubfoot
Hand Deformities, Congenital
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Urogenital Abnormalities
Cryptorchidism
Genetic Diseases, Inborn
Anemia, Hemolytic, Congenital
Thalassemia
alpha-Thalassemia
Dwarfism
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Lysosomal Storage Diseases
Mucopolysaccharidoses
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Mucinoses
Mucopolysaccharidoses
Skin Diseases
Breast Diseases
Gynecomastia
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Mucopolysaccharidoses
Lysosomal Storage Diseases
Mucopolysaccharidoses
Nutrition Disorders
Overnutrition
Obesity
Endocrine System Diseases
Dwarfism
Gonadal Disorders
Hypogonadism
Testicular Diseases
Cryptorchidism
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Sex Chromosome Aberrations
Disease
Syndrome
Disease Attributes
Diseases in Twins
Growth Disorders
Signs and Symptoms
Body Weight
Overweight
Obesity
Failure to Thrive
Neurologic Manifestations
Neurobehavioral Manifestations
Communication Disorders
Language Disorders
Speech Disorders
Intellectual Disability
Neuromuscular Manifestations
Muscle Hypertonia
Muscle Spasticity
Seizures
Sensation Disorders
Hearing Disorders
Hearing Loss
Deafness
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