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210600
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SECKEL SYNDROME 1
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Neoplasms
Neoplasms by Histologic Type
Leukemia
Leukemia, Myeloid
Leukemia, Myeloid, Acute
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Hand Deformities
Hand Deformities, Congenital
Joint Diseases
Hip Dislocation, Congenital
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Holoprosencephaly
Microcephaly
Hip Dislocation, Congenital
Limb Deformities, Congenital
Upper Extremity Deformities, Congenital
Hand Deformities, Congenital
Stomatognathic Diseases
Mouth Diseases
Mouth Abnormalities
Oral Manifestations
Stomatognathic System Abnormalities
Mouth Abnormalities
Tooth Abnormalities
Anodontia
Dental Enamel Hypoplasia
Tooth Diseases
Tooth Abnormalities
Anodontia
Dental Enamel Hypoplasia
Tooth Demineralization
Nervous System Diseases
Nervous System Malformations
Agenesis of Corpus Callosum
Holoprosencephaly
Malformations of Cortical Development
Microcephaly
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Fetal Growth Retardation
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Heart Septal Defects, Ventricular
Heart Diseases
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Heart Septal Defects, Ventricular
Hemic and Lymphatic Diseases
Hematologic Diseases
Anemia
Anemia, Aplastic
Anemia, Hypoplastic, Congenital
Fanconi Anemia
Bone Marrow Diseases
Anemia, Aplastic
Anemia, Hypoplastic, Congenital
Fanconi Anemia
Pancytopenia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Holoprosencephaly
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Heart Septal Defects, Ventricular
Chromosome Disorders
Holoprosencephaly
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Holoprosencephaly
Microcephaly
Hip Dislocation, Congenital
Limb Deformities, Congenital
Hand Deformities, Congenital
Nervous System Malformations
Agenesis of Corpus Callosum
Holoprosencephaly
Holoprosencephaly
Malformations of Cortical Development
Microcephaly
Stomatognathic System Abnormalities
Mouth Abnormalities
Tooth Abnormalities
Anodontia
Dental Enamel Hypoplasia
Fetal Diseases
Fetal Growth Retardation
Genetic Diseases, Inborn
Anemia, Hypoplastic, Congenital
Fanconi Anemia
Chromosome Disorders
Holoprosencephaly
Dwarfism
Nutritional and Metabolic Diseases
Metabolic Diseases
DNA Repair-Deficiency Disorders
Fanconi Anemia
Endocrine System Diseases
Dwarfism
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Trisomy
Chromosomal Instability
Chromosome Fragility
Chromosome Duplication
Trisomy
Disease
Syndrome
Disease Attributes
Facies
Genomic Instability
Chromosomal Instability
Chromosome Fragility
Growth Disorders
Fetal Growth Retardation
Signs and Symptoms
Body Weight
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Oral Manifestations
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