Informaţii despre

Nume Microphthalmia
Pagina Web www.malacards.org
Clasificare globală Malacards Boli fetale; Boli rare
Clasificari ICD10 Microphthalmos
Clasificare anatomică Malacards Boli ale ochiului

Vezi şi

Boli A-Z Ablepharon-Macrostomia Syndrome Adenocarcinoma Adie Pupil Agammaglobulinemia Aging Aicardi Syndrome Albinism Albinism, Ocular, Type I Albinism, Ocular, with Sensorineural Deafness Alexander Disease Alopecia, Neurologic Defects, and Endocrinopathy Syndrome Alport Syndrome, X-Linked Al-Raqad Syndrome Alveolar Capillary Dysplasia Amelogenesis Imperfecta Amelogenesis Imperfecta, Type Ie Androgen Insensitivity Syndrome, Mild Angiomyolipoma Aniridia 1 Anorexia Nervosa 1 Anus, Imperforate Aplasia Cutis Congenita Arrhinia Arthrochalasia Ehlers-Danlos Syndrome Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Autism Autism Spectrum Disorder Axenfeld-Rieger Syndrome, Type 1 Basaloid Follicular Hamartoma Bilateral Retinoblastoma Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex Bleeding Disorder, Platelet-Type, 11 Blood Group--Ahonen Bone Mineral Density Quantitative Trait Locus 15 Bone Mineral Density Quantitative Trait Locus 8 Bosma Arhinia Microphthalmia Syndrome Brachydactyly Branchial Arch Defects Branchiooculofacial Syndrome Branchiootorenal Syndrome Breast Angiosarcoma Cardiomyopathy, Infantile Histiocytoid Carpal Tunnel Syndrome Cataract Cerebellar Hypoplasia Cerebral Atrophy Cerebral Palsy Cerebritis Cervicitis Childhood Kidney Cell Carcinoma Choanal Atresia, Posterior Cholestasis Chondrodysplasia with Platyspondyly, Distinctive Brachydactyly, Hydrocephaly, and Microphthalmia Chorioretinitis Chromosomal Triplication Chromosome 13q14 Deletion Syndrome Chromosome 3p Duplication Chromosome Xp Deletion Chylomicron Retention Disease Clear Cell Sarcoma Cleft Lip Coloboma of Eye Lens Coloboma of Eyelid Coloboma of Macula Coloboma of Optic Nerve Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and Deafness Colobomatous Microphthalmia Combined Pituitary Hormone Deficiency Congenital Aphakia Congenital Cytomegalovirus Congenital Zika Syndrome Conotruncal Heart Malformations Corneal Staphyloma Corpus Callosum, Agenesis of, with Abnormal Genitalia Cortisone Reductase Deficiency 1 Craniotelencephalic Dysplasia Cryptophthalmos Cutaneous Lupus Erythematosus Cutis Laxa, Autosomal Recessive, Type Iiia Dermoid Cyst Dextrocardia Dextrocardia with Unusual Facies and Microphthalmia Diaphragmatic Eventration Diffuse Meningeal Melanocytosis Diphtheria Distal Trisomy 3p Doyne Honeycomb Retinal Dystrophy Dyschromatosis Symmetrica Hereditaria Dysostosis Ectodermal Dysplasia Embryonal Carcinoma Encephalocele Epithelioid Cell Melanoma Esophageal Atresia Fanconi Anemia, Complementation Group E Feingold Syndrome 1 Focal Dermal Hypoplasia Fryns Microphthalmia Syndrome Gallbladder Melanoma Giant Cell Tumor Glucose Transporter Type 1 Deficiency Syndrome Gombo Syndrome Growth Hormone Deficiency Hallermann-Streiff Syndrome Halo Nevi Hard Palate Cancer Helix Syndrome Hemifacial Microsomia Hemimegalencephaly Hepatic Adenomas, Familial Hermansky-Pudlak Syndrome 3 Hermaphroditism Holoprosencephaly Holoprosencephaly 8 Hydranencephaly Hydrocephalus, Nonsyndromic, Autosomal Recessive 2 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant Hyperglycinuria Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypomelanotic Disorder Hypopituitarism Hypospadias Hypotonia Hypotrichosis Hypoxia Immunoglobulin E Concentration, Serum Integumentary System Cancer Isolated Klippel-Feil Syndrome Leukemia Leukocoria Leukodystrophy, Hypomyelinating, 5 Linear Skin Defects with Multiple Congenital Anomalies 1 Lupus Erythematosus Macs Syndrome Malignant Spindle Cell Melanoma Mast Cell Activation Syndrome Mast Cell Disease Mcleod Syndrome Melanoacanthoma Melanoma Melanoma-Astrocytoma Syndrome Melanoma Metastasis Melanotic Neurilemmoma Melkersson-Rosenthal Syndrome Meningocele Microcephaly Microcephaly Microcornea Syndrome Seemanova Type Microphthalmia/anophthalmia/coloboma Spectrum Microphthalmia, Isolated 1 Microphthalmia, Isolated 2 Microphthalmia, Isolated, with Cataract 1 Microphthalmia, Isolated, with Coloboma 4 Microphthalmia, Isolated, with Coloboma 6 Microphthalmia Microtia Fetal Akinesia Microphthalmia, Syndromic 1 Microphthalmia, Syndromic 10 Microphthalmia, Syndromic 2 Microphthalmia, Syndromic 3 Microphthalmia, Syndromic 5 Microphthalmia, Syndromic 8 Microphthalmia, Syndromic 9 Microphthalmia with Limb Anomalies Microtia Muscular Dystrophy Myeloid Leukemia Myopia Nance-Horan Syndrome Nanophthalmos 1 Nanophthalmos 3 Neuroblastoma Neurofibroma Neuronitis Ocular Albinism Oculocerebrocutaneous Syndrome Odontoma Optic Nerve Hypoplasia, Bilateral Orbital Cyst Orofacial Cleft Osteopetrosis Osteoporosis-Pseudoglioma Syndrome Pancreatitis Peritonitis Persistent Hyperplastic Primary Vitreous Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Persistent Mullerian Duct Syndrome, Types I and Ii Phelan-Mcdermid Syndrome Pigmented Basal Cell Carcinoma Polykaryocytosis Inducer Posterior Uveal Melanoma Pycnodysostosis Pyogenic Granuloma Refsum Disease, Classic Retinal Degeneration Retinal Detachment Retinitis Retinoblastoma Retinochoroidal Coloboma Retroperitoneal Sarcoma Richards-Rundle Syndrome Ring Chromosome 14 Syndrome Robinow Syndrome, Autosomal Recessive Sarcoma Sclerocornea Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Skin/hair/eye Pigmentation, Variation in, 3 Skin Tag Sleep Disorder Small Cell Carcinoma Spasticity Split Foot Split Hand Tietz Albinism-Deafness Syndrome Townes-Brocks Syndrome Tyrosinase-Like Undifferentiated Pleomorphic Sarcoma Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 Waardenburg's Syndrome Waardenburg Syndrome, Type 2a Waardenburg Syndrome, Type 2e Waardenburg Syndrome Type 4 Waardenburg Syndrome, Type 4c Walker-Warburg Syndrome Wolf-Hirschhorn Syndrome Woods Syndrome Xp22.3 Microdeletion Syndrome Yemenite Deaf-Blind Hypopigmentation Syndrome