Informaţii despre

Nume Achondroplasia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Achondroplasia
Clasificare anatomică Malacards Boli osoase

Vezi şi

Boli A-Z 47, Xxy Acanthosis Nigricans Achondrogenesis Achondrogenesis, Type Ii Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans Acromesomelic Dysplasia Adie Pupil Aging Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Antley-Bixler Syndrome Apert Syndrome Arachnoid Cysts Arachnoiditis Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Atelosteogenesis Atrichia with Papular Lesions Ayme-Gripp Syndrome Beare-Stevenson Cutis Gyrata Syndrome Biliary Atresia Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Blood Group, Dombrock System Blood Group, I System Body Mass Index Quantitative Trait Locus 10 Body Mass Index Quantitative Trait Locus 11 Body Mass Index Quantitative Trait Locus 12 Body Mass Index Quantitative Trait Locus 14 Body Mass Index Quantitative Trait Locus 18 Body Mass Index Quantitative Trait Locus 4 Body Mass Index Quantitative Trait Locus 7 Body Mass Index Quantitative Trait Locus 8 Body Mass Index Quantitative Trait Locus 9 Bone Development Disease Brittle Bone Disorder Cartilage Disease Cervicitis Chiari Malformation Choanal Atresia, Posterior Chondroblastoma Chondromyxoid Fibroma Chorioretinitis Ciliopathy Cleidocranial Dysplasia Cohen-Gibson Syndrome Cone-Rod Dystrophy 2 Craniosynostosis Crouzon Syndrome Crouzon Syndrome with Acanthosis Nigricans Down Syndrome Duane Retraction Syndrome Dwarfism Endosteal Hyperostosis, Autosomal Dominant Fragile X Syndrome Fundus Albipunctatus Gonadal Dysgenesis Hemifacial Spasm Hepatic Adenomas, Familial Hydrocephalus Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypochondroplasia Hypotonia Idiopathic Hemiconvulsion-Hemiplegia Syndrome Immunoglobulin E Concentration, Serum Infantile Hypotonia Jackson-Weiss Syndrome Keratoconus Lacrimoauriculodentodigital Syndrome Leri-Weill Dyschondrosteosis Leukemia Lipodystrophy, Partial, Acquired Lipomatosis Luteoma Macrocephaly/megalencephaly Syndrome, Autosomal Recessive Marfan Syndrome Megalencephaly Middle Ear Disease Mucositis Muenke Syndrome Multiple Epiphyseal Dysplasia Muscular Dystrophy Myeloid Leukemia Nail-Patella Syndrome Neuroblastoma Neurofibromatosis, Type Iv, of Riccardi Opitz Gbbb Syndrome, Type I Osteoarthritis Osteoarthritis with Mild Chondrodysplasia Osteochondritis Dissecans Osteochondrodysplasia Osteoglophonic Dysplasia Papilledema Pectus Excavatum Pelvic Lipomatosis Pelvic Organ Prolapse Periodontal Disease Periodontitis Pfeiffer Syndrome Pharyngitis Pitt-Hopkins Syndrome Plagiocephaly Polydactyly Polyhydramnios Porphyria Pseudoachondroplasia Pulmonary Hypertension Radioulnar Synostosis Renal Glucosuria Renal Osteodystrophy Retinitis Saethre-Chotzen Syndrome Scoliosis Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Skeletal Dysplasias Sleep Apnea Sleep Disorder Spinal Cord Injury Spinal Disease Spinal Stenosis Spondylitis Spondyloarthropathy 1 Spondyloepiphyseal Dysplasia Congenita Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations Spondylosis Synostosis Synovial Chondromatosis Syringomyelia Teeth, Supernumerary Tetralogy of Fallot Thanatophoric Dysplasia, Type I Thanatophoric Dysplasia, Type Ii Three M Syndrome 1 Thrombocytopenia Trigeminal Neuralgia Undifferentiated Pleomorphic Sarcoma Ventricular Septal Defect