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Query OMIM entry list
600584
NKX2E
NK2, DROSOPHILA, HOMOLOG OF, E
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Neoplasms
Hamartoma
Hamartoma Syndrome, Multiple
Proteus Syndrome
Neoplasms by Histologic Type
Neoplasms, Nerve Tissue
Nerve Sheath Neoplasms
Neurofibroma
Neurofibromatoses
Neoplasms, Multiple Primary
Hamartoma Syndrome, Multiple
Proteus Syndrome
Neoplastic Syndromes, Hereditary
Neurofibromatoses
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Congenital Hypothyroidism
Osteochondrodysplasias
Fibrous Dysplasia of Bone
Fibrous Dysplasia, Polyostotic
Proteus Syndrome
Bone Diseases, Endocrine
Congenital Hypothyroidism
Hand Deformities
Hand Deformities, Congenital
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Ectromelia
Proteus Syndrome
Upper Extremity Deformities, Congenital
Hand Deformities, Congenital
Nervous System Diseases
Neurocutaneous Syndromes
Neurofibromatoses
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Neurofibromatoses
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Tetralogy of Fallot
Heart Diseases
Arrhythmias, Cardiac
Heart Block
Cardiomyopathies
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Tetralogy of Fallot
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Incontinentia Pigmenti
Proteus Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Tetralogy of Fallot
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Ectromelia
Hand Deformities, Congenital
Proteus Syndrome
Situs Inversus
Skin Abnormalities
Incontinentia Pigmenti
Genetic Diseases, Inborn
Dwarfism
Congenital Hypothyroidism
Heredodegenerative Disorders, Nervous System
Neurofibromatoses
Neoplastic Syndromes, Hereditary
Neurofibromatoses
Skin Diseases, Genetic
Incontinentia Pigmenti
Skin and Connective Tissue Diseases
Skin Diseases
Pigmentation Disorders
Incontinentia Pigmenti
Skin Abnormalities
Incontinentia Pigmenti
Skin Diseases, Genetic
Incontinentia Pigmenti
Endocrine System Diseases
Dwarfism
Congenital Hypothyroidism
Thyroid Diseases
Hypothyroidism
Congenital Hypothyroidism
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Arrhythmias, Cardiac
Heart Block
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Disease Attributes
Disease Progression
Recurrence
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