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115150
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CARDIOFACIOCUTANEOUS SYNDROME
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Neoplasms
Neoplasms by Histologic Type
Leukemia
Leukemia, Lymphoid
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Neoplasms, Nerve Tissue
Nerve Sheath Neoplasms
Neurofibroma
Neurofibromatoses
Neurofibromatosis 1
Neoplasms, Vascular Tissue
Hemangioma
Neoplasms by Site
Skin Neoplasms
Neoplastic Syndromes, Hereditary
Neurofibromatoses
Neurofibromatosis 1
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Marfan Syndrome
Spinal Diseases
Spinal Curvatures
Scoliosis
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Noonan Syndrome
Digestive System Diseases
Digestive System Abnormalities
Nervous System Diseases
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Neurocutaneous Syndromes
Neurofibromatoses
Neurofibromatosis 1
Neurodegenerative Diseases
Heredodegenerative Disorders, Nervous System
Neurofibromatoses
Neurofibromatosis 1
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Mental Retardation, X-Linked
Neuromuscular Manifestations
Muscle Hypotonia
Neuromuscular Diseases
Peripheral Nervous System Diseases
Neurofibromatosis 1
Eye Diseases
Eye Abnormalities
Eyelid Diseases
Blepharoptosis
Male Urogenital Diseases
Genital Diseases, Male
Testicular Diseases
Cryptorchidism
Urogenital Abnormalities
Cryptorchidism
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Cardiovascular Diseases
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Heart Septal Defects, Ventricular
Marfan Syndrome
Noonan Syndrome
Heart Diseases
Cardiomyopathies
Cardiomyopathy, Hypertrophic
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Heart Septal Defects, Ventricular
Marfan Syndrome
Noonan Syndrome
Heart Valve Diseases
Aortic Valve Stenosis
Aortic Stenosis, Subvalvular
Cardiomyopathy, Hypertrophic
Mitral Valve Insufficiency
Pulmonary Valve Stenosis
Ventricular Outflow Obstruction
Pulmonary Valve Stenosis
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
Lymphatic Diseases
Lymphoproliferative Disorders
Leukemia, Lymphoid
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Ectodermal Dysplasia
Marfan Syndrome
Cardiovascular Abnormalities
Heart Defects, Congenital
Heart Septal Defects
Heart Septal Defects, Atrial
Heart Septal Defects, Ventricular
Marfan Syndrome
Noonan Syndrome
Digestive System Abnormalities
Eye Abnormalities
Musculoskeletal Abnormalities
Craniofacial Abnormalities
Microcephaly
Noonan Syndrome
Nervous System Malformations
Malformations of Cortical Development
Microcephaly
Skin Abnormalities
Ectodermal Dysplasia
Urogenital Abnormalities
Cryptorchidism
Fetal Diseases
Erythroblastosis, Fetal
Hydrops Fetalis
Genetic Diseases, Inborn
Genetic Diseases, X-Linked
Mental Retardation, X-Linked
Hemoglobinopathies
Thalassemia
alpha-Thalassemia
Hydrops Fetalis
Heredodegenerative Disorders, Nervous System
Mental Retardation, X-Linked
Neurofibromatoses
Neurofibromatosis 1
Marfan Syndrome
Neoplastic Syndromes, Hereditary
Neurofibromatoses
Neurofibromatosis 1
Skin Diseases, Genetic
Dermatitis, Atopic
Ectodermal Dysplasia
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Marfan Syndrome
Noonan Syndrome
Skin Diseases
Dermatitis
Dermatitis, Atopic
Dermatitis, Seborrheic
Erythema
Facial Dermatoses
Hair Diseases
Keratosis
Pigmentation Disorders
Hyperpigmentation
Melanosis
Lentigo
Sebaceous Gland Diseases
Dermatitis, Seborrheic
Skin Abnormalities
Ectodermal Dysplasia
Skin Diseases, Eczematous
Dermatitis, Atopic
Dermatitis, Seborrheic
Skin Diseases, Genetic
Dermatitis, Atopic
Ectodermal Dysplasia
Skin Diseases, Papulosquamous
Dermatitis, Seborrheic
Skin Neoplasms
Endocrine System Diseases
Gonadal Disorders
Testicular Diseases
Cryptorchidism
Immune System Diseases
Blood Group Incompatibility
Erythroblastosis, Fetal
Hydrops Fetalis
Hypersensitivity
Hypersensitivity, Immediate
Dermatitis, Atopic
Immunoproliferative Disorders
Lymphoproliferative Disorders
Leukemia, Lymphoid
Precursor Cell Lymphoblastic Leukemia-Lymphoma
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Hypertrophy
Splenomegaly
Nails, Malformed
Pathologic Processes
Chromosome Aberrations
Aneuploidy
Monosomy
Chromosome Deletion
Disease
Syndrome
Disease Attributes
Diseases in Twins
Facies
Growth Disorders
Signs and Symptoms
Edema
Hydrops Fetalis
Failure to Thrive
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Neuromuscular Manifestations
Muscle Hypotonia
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