MeSH Treeview
Query OMIM entry list
302960
CDPX2
CHONDRODYSPLASIA PUNCTATA 2, X-LINKED DOMINANT
→
High-scoring List
Musculoskeletal Diseases
Bone Diseases
Bone Diseases, Developmental
Osteochondrodysplasias
Chondrodysplasia Punctata
Chondrodysplasia Punctata, Rhizomelic
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Nervous System Diseases
Central Nervous System Diseases
Brain Diseases
Epilepsy
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Eye Diseases
Eye Abnormalities
Lens Diseases
Cataract
Female Urogenital Diseases and Pregnancy Complications
Pregnancy Complications
Fetal Death
Obstetric Labor Complications
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital Abnormalities
Abnormalities, Multiple
Incontinentia Pigmenti
Smith-Lemli-Opitz Syndrome
Chromosome Disorders
Eye Abnormalities
Musculoskeletal Abnormalities
Limb Deformities, Congenital
Skin Abnormalities
Ichthyosis
Ichthyosis, X-Linked
Incontinentia Pigmenti
Genetic Diseases, Inborn
Chromosome Disorders
Genetic Diseases, X-Linked
Ichthyosis, X-Linked
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Smith-Lemli-Opitz Syndrome
Peroxisomal Disorders
Chondrodysplasia Punctata, Rhizomelic
Steroid Metabolism, Inborn Errors
Ichthyosis, X-Linked
Smith-Lemli-Opitz Syndrome
Skin Diseases, Genetic
Ichthyosis, X-Linked
Incontinentia Pigmenti
Infant, Newborn, Diseases
Asphyxia Neonatorum
Ichthyosis
Ichthyosis, X-Linked
Skin and Connective Tissue Diseases
Skin Diseases
Dermatitis
Dermatitis, Exfoliative
Hair Diseases
Hypotrichosis
Alopecia
Alopecia Areata
Keratosis
Ichthyosis
Ichthyosis, X-Linked
Pigmentation Disorders
Incontinentia Pigmenti
Skin Abnormalities
Ichthyosis
Ichthyosis, X-Linked
Incontinentia Pigmenti
Skin Diseases, Eczematous
Dermatitis, Exfoliative
Skin Diseases, Genetic
Ichthyosis, X-Linked
Incontinentia Pigmenti
Skin Diseases, Papulosquamous
Psoriasis
Nutritional and Metabolic Diseases
Metabolic Diseases
Lipid Metabolism Disorders
Dyslipidemias
Smith-Lemli-Opitz Syndrome
Lipid Metabolism, Inborn Errors
Metabolism, Inborn Errors
Lipid Metabolism, Inborn Errors
Smith-Lemli-Opitz Syndrome
Peroxisomal Disorders
Chondrodysplasia Punctata, Rhizomelic
Steroid Metabolism, Inborn Errors
Ichthyosis, X-Linked
Smith-Lemli-Opitz Syndrome
Animal Diseases
Rodent Diseases
Pathological Conditions, Signs and Symptoms
Pathological Conditions, Anatomical
Alopecia
Atrophy
Nails, Malformed
Pathologic Processes
Chromosome Aberrations
Ring Chromosomes
Sex Chromosome Aberrations
Translocation, Genetic
Death
Fetal Death
Disease
Syndrome
Fibrosis
Signs and Symptoms
Neurologic Manifestations
Neurobehavioral Manifestations
Intellectual Disability
Database Center for Life Science
