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308700
KAL1
KALLMANN SYNDROME 1
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Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Osteochondrodysplasias
Chondrodysplasia Punctata
Bone Diseases, Metabolic
Osteoporosis
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Hypothalamic Diseases
Pituitary Diseases
Hypopituitarism
Movement Disorders
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Paralysis
Hemiplegia
Sensation Disorders
Olfaction Disorders
Vision Disorders
Color Vision Defects
Eye Diseases
Vision Disorders
Color Vision Defects
Male Urogenital Diseases
Genital Diseases, Male
Infertility
Infertility, Male
Testicular Diseases
Cryptorchidism
Urogenital Abnormalities
Cryptorchidism
Disorders of Sex Development
46, XY Disorders of Sex Development
Kallmann Syndrome
Gonadal Dysgenesis
Turner Syndrome
Sex Chromosome Disorders of Sex Development
Turner Syndrome
Female Urogenital Diseases and Pregnancy Complications
Female Urogenital Diseases
Urogenital Abnormalities
Disorders of Sex Development
46, XY Disorders of Sex Development
Kallmann Syndrome
Gonadal Dysgenesis
Turner Syndrome
Sex Chromosome Disorders of Sex Development
Turner Syndrome
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Turner Syndrome
Heart Diseases
Heart Defects, Congenital
Turner Syndrome
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Coagulation Disorders
Blood Coagulation Disorders, Inherited
Hemophilia A
Coagulation Protein Disorders
Hemophilia A
Hemorrhagic Disorders
Hemophilia A
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Cardiovascular Abnormalities
Heart Defects, Congenital
Turner Syndrome
Chromosome Disorders
Sex Chromosome Disorders
Sex Chromosome Disorders of Sex Development
Turner Syndrome
Skin Abnormalities
Ichthyosis
Ichthyosis, X-Linked
Urogenital Abnormalities
Cryptorchidism
Disorders of Sex Development
46, XY Disorders of Sex Development
Kallmann Syndrome
Gonadal Dysgenesis
Turner Syndrome
Sex Chromosome Disorders of Sex Development
Turner Syndrome
Genetic Diseases, Inborn
Blood Coagulation Disorders, Inherited
Hemophilia A
Chromosome Disorders
Sex Chromosome Disorders
Sex Chromosome Disorders of Sex Development
Turner Syndrome
Genetic Diseases, X-Linked
Ichthyosis, X-Linked
Kallmann Syndrome
Metabolism, Inborn Errors
Steroid Metabolism, Inborn Errors
Ichthyosis, X-Linked
Skin Diseases, Genetic
Ichthyosis, X-Linked
Infant, Newborn, Diseases
Ichthyosis
Ichthyosis, X-Linked
Skin and Connective Tissue Diseases
Skin Diseases
Keratosis
Ichthyosis
Ichthyosis, X-Linked
Skin Abnormalities
Ichthyosis
Ichthyosis, X-Linked
Skin Diseases, Genetic
Ichthyosis, X-Linked
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Steroid Metabolism, Inborn Errors
Ichthyosis, X-Linked
Endocrine System Diseases
Gonadal Disorders
Disorders of Sex Development
46, XY Disorders of Sex Development
Kallmann Syndrome
Gonadal Dysgenesis
Turner Syndrome
Sex Chromosome Disorders of Sex Development
Turner Syndrome
Hypogonadism
Eunuchism
Kallmann Syndrome
Puberty, Delayed
Testicular Diseases
Cryptorchidism
Pituitary Diseases
Hypopituitarism
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Sex Chromosome Aberrations
Translocation, Genetic
Disease
Syndrome
Disease Attributes
Disease Susceptibility
Genetic Predisposition to Disease
Diseases in Twins
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Paralysis
Hemiplegia
Sensation Disorders
Olfaction Disorders
Vision Disorders
Color Vision Defects
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