Informaţii despre

Nume Coloboma of Macula
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli rare
Clasificari ICD10 Coloboma of iris; Other congenital malformations of posterior segment of eye
Clasificare anatomică Malacards Boli ale ochiului

Vezi şi

Boli A-Z Achondroplasia Acrofacial Dysostosis Acrofacial Dysostosis 1, Nager Type Acrofrontofacionasal Dysostosis Acute Closed-Angle Glaucoma Adenoma Aging Albinism Al-Gazali-Bakalinova Syndrome Alobar Holoprosencephaly Alopecia Alopecia, Congenital Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alveolar Capillary Dysplasia Amblyopia Amelogenesis Imperfecta Amniotic Band Syndrome Aniridia 1 Anorexia Nervosa 1 Anterior Segment Dysgenesis 1 Anus, Imperforate Arachnoiditis Arteriovenous Malformation Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 2a Arthrogryposis, Distal, Type 9 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 Astigmatism Ataxia and Polyneuropathy, Adult-Onset Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Attention Deficit-Hyperactivity Disorder Axenfeld-Rieger Syndrome, Type 1 Baraitser-Winter Syndrome Baraitser-Winter Syndrome 1 Bardet-Biedl Syndrome 14 Biemond Syndrome Biemond Syndrome Ii Bilateral Retinoblastoma Blepharophimosis Blood Group--Ahonen Body Dysmorphic Disorder 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 Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Brachydactyly Brachydactyly, Coloboma, and Anterior Segment Dysgenesis Branchiootorenal Syndrome Capillary Hemangioma Cataract Cat Eye Syndrome Cerebritis Charge Syndrome Choanal Atresia, Posterior Chondrodysplasia Punctata Syndrome Chorioretinitis Choroiditis Chromosomal Triplication Chromosome 16p13.3 Deletion Syndrome, Proximal Cleft Lip Cleft Lip/palate Clubfoot Coloboma, Congenital Heart Disease, Ichthyosiform Dermatosis, Mental Retardation, and Ear Anomalies Syndrome Coloboma, Ocular, Autosomal Dominant Coloboma, Ocular, with or Without Hearing Impairment, Cleft Lip/palate, and/or Mental Retardation Coloboma of Eye Lens Coloboma of Eyelid Coloboma of Iris Coloboma of Macula with Type B Brachydactyly Coloboma of Optic Nerve Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and Deafness Colobomatous Microphthalmia Combined Hamartoma of the Retina and Retinal Pigment Epithelium Congenital Aphakia Congenital Contractures Congenital Disorder of Glycosylation, Type Iq Congenital Ectropion Uveae Corneal Edema Cryptophthalmos Cutaneous Mastocytosis Cutis Laxa, Autosomal Recessive, Type Iiia Diabetes Insipidus Dobrow Syndrome Down Syndrome Dwarfism Dysostosis Ectropion Encephalocele Encephalocraniocutaneous Lipomatosis Endotheliitis Entropion Epilepsy Esophageal Atresia Esotropia Exophthalmos Fanconi Anemia, Complementation Group E Fryns Microphthalmia Syndrome Galactose Epimerase Deficiency Glomerulonephritis Goldberg-Shprintzen Syndrome Graves' Disease Grouped Pigmentation of the Retina Hemangioma Hemifacial Microsomia Hepatitis Holoprosencephaly Hyaline Fibromatosis Syndrome Hydranencephaly Hydrocephalus Hydrolethalus Syndrome 1 Hydronephrosis Hydrops, Lactic Acidosis, and Sideroblastic Anemia Hypertelorism Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypogonadism Hypomelanosis of Ito Hypospadias Hypospadias, Hypertelorism, Upper Lid Coloboma, and Mixed-Type Hearing Loss Ichthyosis Idiopathic Hypercalciuria Inner Ear Disease Isolated Ectopia Lentis Isolated Klippel-Feil Syndrome Johnson Neuroectodermal Syndrome Keratoconus Keratomalacia Klippel-Feil Syndrome Laryngomalacia Learning Disability Leber Congenital Amaurosis 5 Lens Disease Lens Subluxation Leukocoria Limbal Stem Cell Deficiency Limb-Body Wall Complex Lipomatosis Loose Anagen Hair Syndrome Macrostomia, Isolated Macular Holes Manitoba Oculotrichoanal Syndrome Marden-Walker Syndrome Marfan Syndrome Mast Cell Activation Syndrome Maxillonasal Dysplasia, Binder Type Megacolon Megalocornea Melanoma Microcephaly Microphthalmia Microphthalmia, Isolated 1 Microphthalmia, Isolated 2 Microphthalmia, Isolated, with Coloboma 1 Microphthalmia, Isolated, with Coloboma 2 Microphthalmia, Isolated, with Coloboma 6 Microtia Morning Glory Syndrome Mosaic Trisomy 8 Moyamoya Disease 1 Myopia Nasopalpebral Lipoma-Coloboma Syndrome Nephronophthisis Neurofibromatosis, Type Iv, of Riccardi Neuronitis Neuroretinitis Nevus, Epidermal Ocular Hypertension Oculocutaneous Albinism Optic Nerve Hypoplasia, Bilateral Orbital Cyst Osteopetrosis Papillorenal Syndrome Pax2-Related Disorder Persistent Hyperplastic Primary Vitreous Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Peters-Plus Syndrome Phace Syndrome Poland Syndrome Polydactyly Porencephaly Primary Angle-Closure Glaucoma Ptosis Renal Dysplasia Renal Hypoplasia Retinal Aplasia Retinal Degeneration Retinal Detachment Retinitis Retinitis Pigmentosa Retinoblastoma Retinochoroidal Coloboma Ring Chromosome 14 Syndrome Ring Chromosome 3 Ritscher-Schinzel Syndrome Scleral Staphyloma Sclerocornea Scoliosis Sensorineural Hearing Loss Situs Inversus Skin Tag Split Foot Split Hand Spondyloocular Syndrome Strabismus Striatal Degeneration, Autosomal Dominant 2 Syngnathia Synostosis Tay-Sachs Disease Telecanthus Temtamy Syndrome Teratoma Tetraploidy Three M Syndrome 1 Undifferentiated Pleomorphic Sarcoma Usher Syndrome Uveal Coloboma-Cleft Lip and Palate-Intellectual Disability Valproate Embryopathy Van Den Ende-Gupta Syndrome Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 West Syndrome White Sponge Nevus 1 Wolf-Hirschhorn Syndrome