MeSH Treeview
Query OMIM entry list
219200
-
CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE II
→
High-scoring List
Bacterial Infections and Mycoses
Bacterial Infections
Gram-Negative Bacterial Infections
Campylobacter Infections
Neoplasms
Neoplasms by Histologic Type
Neoplasms, Glandular and Epithelial
Neoplasms, Squamous Cell
Papilloma
Neoplasms by Site
Bone Neoplasms
Skull Neoplasms
Nose Neoplasms
Head and Neck Neoplasms
Otorhinolaryngologic Neoplasms
Nose Neoplasms
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Dwarfism
Bone Diseases, Metabolic
Osteoporosis
Bone Neoplasms
Skull Neoplasms
Nose Neoplasms
Joint Diseases
Hip Dislocation, Congenital
Musculoskeletal Abnormalities
Hip Dislocation, Congenital
Respiratory Tract Diseases
Nose Diseases
Nose Neoplasms
Respiratory Tract Neoplasms
Nose Neoplasms
Otorhinolaryngologic Diseases
Nose Diseases
Nose Neoplasms
Otorhinolaryngologic Neoplasms
Nose Neoplasms
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Cerebellar Diseases
Dandy-Walker Syndrome
Epilepsy
Status Epilepticus
Hydrocephalus
Dandy-Walker Syndrome
Intracranial Hypertension
Hydrocephalus
Dandy-Walker Syndrome
Nervous System Malformations
Dandy-Walker Syndrome
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Diseases
Fetal Growth Retardation
Hemic and Lymphatic Diseases
Hematologic Diseases
Blood Protein Disorders
Agammaglobulinemia
Leukocyte Disorders
Leukopenia
Lymphatic Diseases
Lymphoproliferative Disorders
Agammaglobulinemia
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Chromosome Disorders
Musculoskeletal Abnormalities
Hip Dislocation, Congenital
Nervous System Malformations
Dandy-Walker Syndrome
Skin Abnormalities
Fetal Diseases
Fetal Growth Retardation
Genetic Diseases, Inborn
Chromosome Disorders
Dwarfism
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Skin Diseases, Genetic
Cutis Laxa
Skin and Connective Tissue Diseases
Connective Tissue Diseases
Cutis Laxa
Skin Diseases
Skin Abnormalities
Skin Diseases, Genetic
Cutis Laxa
Nutritional and Metabolic Diseases
Metabolic Diseases
Metabolism, Inborn Errors
Carbohydrate Metabolism, Inborn Errors
Endocrine System Diseases
Dwarfism
Immune System Diseases
Immunologic Deficiency Syndromes
Agammaglobulinemia
Pathological Conditions, Signs and Symptoms
Pathologic Processes
Chromosome Aberrations
Disease
Syndrome
Growth Disorders
Fetal Growth Retardation
Signs and Symptoms
Body Weight
Birth Weight
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Database Center for Life Science
