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278250
WSS
WRINKLY SKIN SYNDROME
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Bacterial Infections and Mycoses
Bacterial Infections
Gram-Negative Bacterial Infections
Campylobacter Infections
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Metabolic
Osteoporosis
Joint Diseases
Hip Dislocation, Congenital
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Hip Dislocation, Congenital
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebrovascular Disorders
Carotid Artery Diseases
Moyamoya Disease
Intracranial Arterial Diseases
Cerebral Arterial Diseases
Moyamoya Disease
Stroke
Epilepsy
Status Epilepticus
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Eye Diseases
Refractive Errors
Myopia
Retinal Diseases
Retinitis
Chorioretinitis
Uveal Diseases
Choroid Diseases
Choroiditis
Chorioretinitis
Uveitis
Panuveitis
Uveitis, Posterior
Choroiditis
Chorioretinitis
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Heart Diseases
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Vascular Diseases
Arterial Occlusive Diseases
Moyamoya Disease
Cerebrovascular Disorders
Carotid Artery Diseases
Moyamoya Disease
Intracranial Arterial Diseases
Cerebral Arterial Diseases
Moyamoya Disease
Stroke
Hemostatic Disorders
Ehlers-Danlos Syndrome
Hemic and Lymphatic Diseases
Hematologic Diseases
Hemorrhagic Disorders
Hemostatic Disorders
Ehlers-Danlos Syndrome
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Hip Dislocation, Congenital
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Skin Abnormalities
Ehlers-Danlos Syndrome
Genetic Diseases, Inborn
Skin Diseases, Genetic
Cutis Laxa
Ehlers-Danlos Syndrome
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Collagen Diseases
Ehlers-Danlos Syndrome
Cutis Laxa
Skin Diseases
Skin Abnormalities
Ehlers-Danlos Syndrome
Skin Diseases, Genetic
Cutis Laxa
Ehlers-Danlos Syndrome
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Growth Disorders
Signs and Symptoms
Body Weight
Birth Weight
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
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