11501 to 11600 most common queries

List represents a sample of symptoms, diseases, and other queries. Updated weekly.

• Spastic Paraplegia - Nephritis - Deafness Syndrome
• Partington-Anderson Syndrome
• Spastic Paraplegia - Precocious Puberty Syndrome
• Serpentine Fibula - Polycystic Kidneys Syndrome
• Iniencephaly
• Pelvic Dysplasia-Arthrogryposis of Lower Limbs Syndrome
• Neural Tube Defects, X-Linked
• Camptodactyly - Arthropathy - Coxa Vara - Pericarditis Syndrome
• Congenital Pericardium Anomaly
• Pfeiffer-Palm-Teller Syndrome
• Isolated Spina Bifida
• Short Stature - Wormian Bones - Dextrocardia Syndrome
• Chitayat Meunier Hodgkinson Syndrome
• Pili Torti - Onychodysplasia Syndrome
• Pili Torti - Developmental Delay - Neurological Abnormalities Syndrome
• Arnold-Chiari Malformation Type 1
• Pilotto Syndrome
• Pinsky - Di George - Harley Syndrome
• Phocomelia Type Schinzel
• Cutaneous Photosensitivity - Lethal Colitis Syndrome
• Piebald Trait - Neurologic Defects Syndrome
• X-Linked Intellectual Disability-Psychosis-Macroorchidism Syndrome
• Severe X-Linked Intellectual Disability Type Gustavson
• Rhizomelic Syndrome Type Urbach
• Congenital Partial Pulmonary Venous Return Anomaly
• Retinohepatoendocrinologic Syndrome
• Robinow-Sorauf Syndrome
• Rombo Syndrome
• Schinzel-Giedion Syndrome
• Say Barber Miller Syndrome
• Familial Pterygium of the Conjunctiva
• Uniparental Disomy of Chromosome 21
• Ptosis - Strabismus - Ectopic Pupils Syndrome
• Ptosis - Vocal Cord Paralysis Syndrome
• Moderately-Differentiated Thymic Neuroendocrine Carcinoma
• Qazi-Markouizos Syndrome
• Congenital Smooth Muscle Hamartoma
• Radio-Renal Syndrome
• Rambaud-Gallian Syndrome
• Congenital Disorder of Glycosylation Type 1o
• Rasmussen Johnsen Thomsen Syndrome
• RAPADILINO Syndrome
• Congenital Bilateral Megacalycosis
• Growth Delay-Hydrocephaly-Lung Hypoplasia Syndrome
• X Chromosome Anomaly
• Young Simpson Syndrome
• X-Linked Intellectual Disability - Seizures - Psoriasis Syndrome
• Y Chromosomal Anomaly
• Syndesmodysplasic Dwarfism
• Osteoglophonic Dwarfism
• Bird-Headed Dwarfism Type Montreal
• Trisomy 17p
• Monosomy 9p
• Myelocerebellar Disorder
• Moore-Federman Syndrome
• Mononen-Karnes-Senac Syndrome
• Microspherophakia - Metaphyseal Dysplasia Syndrome
• Autosomal Dominant Microcephaly
• Metachondromatosis
• Gestational Trophoblastic Disease
• Epithelioid Trophoblastic Tumor
• Partial Pancreatic Agenesis
• Parana Hard-Skin Syndrome
• Familial Recurrent Peripheral Facial Palsy
• Spastic Paraplegia-Glaucoma-Intellectual Disability Syndrome
• Spastic Paraparesis-Deafness Syndrome
• Infantile Malignant Osteopetrosis
• Autosomal Recessive Osteopetrosis Type 2
• Autosomal Dominant Osteosclerosis Type Worth
• Lateral Meningocele Syndrome
• Pachydermoperiostosis, Autosomal Dominant
• Otoonychoperoneal Syndrome
• Progressive Osseous Heteroplasia
• Osteomesopyknosis
• Lichen Planopilaris
• Rare Cutaneous Lichen Planus
• Onycho-Tricho-Dysplasia-Neutropenia Syndrome
• Tumor of Meninges
• Ophthalmoplegia-Intellectual Disability-Lingua Scrotalis Syndrome
• Malignant Perineurioma
• Autosomal Recessive Sideroblastic Anemia
• Odontomatosis - Aortae Esophagus Stenosis Syndrome
• Odonto-Onycho-Dermal Dysplasia
• Oculo-Cerebral Hypopigmentation Syndrome Type Preus
• Oculocerebral Hypopigmentation Syndrome Type Cross
• Oculocerebral Dysplasia
• Oculotrichodysplasia
• Oculorenocerebellar Syndrome
• Oculo-Palato-Cerebral Syndrome
• Oligomeganephronia
• Idiopathic Recurrent Pericarditis
• MASS Syndrome
• Neuronal Intranuclear Inclusion Disease
• Congenital Velopharyngeal Incompetence
• Parietal Foramina with Cleidocranial Dysplasia
• Pigmented Paravenous Retinochoroidal Atrophy
• Rare Tumor of Neuroepithelial Tissue
• Sickle Cell - Beta-Thalassemia
• Pancreatic Hypoplasia - Diabetes - Congenital Heart Disease Syndrome
• Thumb Deformity - Alopecia - Pigmentation Anomaly Syndrome