Informaţii despre

Nume Blepharophimosis
Pagina Web www.malacards.org
Clasificare globală Malacards Boli rare
Clasificare anatomică Malacards Boli ale ochiului

Vezi şi

Boli A-Z 3mc Syndrome Acroosteolysis Aging Albright's Hereditary Osteodystrophy Alopecia Alopecia Areata Al-Raqad Syndrome Amblyopia Amenorrhea Aniridia 1 Anorexia Nervosa 1 Arthrochalasia Ehlers-Danlos Syndrome Arthrogryposis, Distal, Type 2a Arthrogryposis, Distal, Type 9 Arthrogryposis Multiplex Congenita, Neurogenic, with Myelin Defect Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Axenfeld-Rieger Syndrome Ayme-Gripp Syndrome Baraitser-Winter Syndrome 1 Blepharophimosis Intellectual Disability Syndromes Blepharophimosis, Ptosis, and Epicanthus Inversus Blepharospasm Blood Group--Ahonen Brachydactyly Cataract Chromosomal Triplication Chromosome 10q Duplication Chromosome 3q Deletion Clubfoot Congenital Contractures Congenital Hypothyroidism Congenital Ptosis Corpus Callosum, Agenesis of Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia Dubowitz Syndrome Dwarfism Epicanthus Epilepsy Esotropia Eyelid Disease Facial Dysmorphism-Anorexia-Cachexia-Eye and Skin Anomalies Syndrome Fanconi Anemia, Complementation Group E Gingivitis Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies Goldberg-Shprintzen Syndrome Hepatic Adenomas, Familial Hydronephrosis Hypertelorism Hypertonia Hypogonadism Hypotonia Infertility Isolated Duane Retraction Syndrome Jorgenson Lenz Syndrome Kaufman Oculocerebrofacial Syndrome Krieble Bixler Syndrome Lacrimal Duct Defect Marden-Walker Syndrome Microcephaly Microcephaly, Autosomal Dominant Myopathy Myotonia Myotonic Dystrophy Ohdo Syndrome Ohdo Syndrome, Sbbys Variant Optic Nerve Hypoplasia, Bilateral Ovarian Cyst Persistent Hyperplastic Primary Vitreous, Autosomal Recessive Polydactyly Polykaryocytosis Inducer Precocious Puberty Premature Menopause Premature Ovarian Failure 1 Propionic Acidemia Ptosis Radioulnar Synostosis Refractive Error Retinitis Retinitis Pigmentosa Serpin Peptidase Inhibitor, Clade a, Member 2, Pseudogene Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Simpson-Golabi-Behmel Syndrome Spastic Diplegia Spasticity Spondyloocular Syndrome Strabismus Synostosis Syringomyelia Telecanthus Three M Syndrome 1 Van Den Ende-Gupta Syndrome Ventricular Septal Defect Vestibular Nystagmus Wisconsin Syndrome