Informaţii despre

Nume Chromosome 16p13.3 Deletion Syndrome, Proximal
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli genetice; Boli rare
Clasificari ICD10 Congenital malformation syndromes predominantly involving limbs
Clasificare anatomică Malacards Boli ale ochiului; Boli endocrine; Boli nefrologice (ale rinichilor); Boli neuronale; Boli osoase; Boli psihice

Vezi şi

Boli A-Z Ablepharon-Macrostomia Syndrome Acute Leukemia Acute Myeloid Leukemia with T(8;16)(p11;p13) Translocation Adie Pupil Aging Alacrima, Achalasia, and Mental Retardation Syndrome Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Anterior Segment Dysgenesis 1 Arthrochalasia Ehlers-Danlos Syndrome Autism Autosomal Dominant Disease Ayme-Gripp Syndrome B Cell Deficiency Blood Group--Ahonen Blood Group, Dombrock 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 Brachydactyly Cerebellar Atrophy, Developmental Delay, and Seizures Cervical Dermoid Cyst Cervicitis Chiari Malformation Chromosomal Triplication Churg-Strauss Syndrome Colorblindness, Partial, Protan Series Congenital Dislocation of the Patella Congenital Hypothyroidism Congenital Tracheal Stenosis Cornelia De Lange Syndrome Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia Dermoid Cyst Duane Retraction Syndrome Echolalia Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome Familial Mediterranean Fever Fanconi Anemia, Complementation Group E Floating-Harbor Syndrome Follicular Lymphoma Frontonasal Dysplasia 1 Gastritis Gastroesophageal Reflux Germ Cells Tumors Growth Hormone Deficiency Hemangioma Hepatic Adenomas, Familial Hepatitis Hepatoblastoma Human T-Cell Leukemia Virus Type 1 Human T-Cell Leukemia Virus Type 2 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypoglycemia Hypotonia Immunodeficiency, Common Variable, 10 Juvenile Glaucoma Keloids Kimura Disease Kniest Dysplasia Laryngitis Leukemia Leukemia, Acute Monocytic Lymphoma Medulloblastoma Megacolon Meningoencephalitis Microcephaly Mosaic Variegated Aneuploidy Syndrome 1 Myopia Myositis Myositis Ossificans Nasopharyngitis Neonatal Leukemia Nephrotic Syndrome Neuroblastoma Otopalatodigital Syndrome, Type I Otopalatodigital Syndrome, Type Ii Ovarian Cyst Periodontal Disease Periodontitis Pheochromocytoma Pilomatrixoma Pituitary Hypoplasia Polydactyly Polymicrogyria, Bilateral Perisylvian, X-Linked Primary Agammaglobulinemia Pulmonary Hypertension Retinal Detachment Retinitis Rett Syndrome Rhabdomyosarcoma Rothmund-Thomson Syndrome Rubinstein-Taybi Syndrome 1 Scoliosis Sex Cord-Gonadal Stromal Tumor Sleep Apnea Slipped Capital Femoral Epiphysis Smith-Lemli-Opitz Syndrome Spondylolisthesis Spondyloocular Syndrome Striate Palmoplantar Keratoderma Thyroiditis Tracheal Stenosis Tricuspid Atresia