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Term:
Rodrigues Blindness (DOID:9008546)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0)
Parent Terms Term With Siblings Child Terms
blindness +     
Growth Disorders +     
hair disease +     
3p- syndrome 
Acid-Labile Subunit Deficiency  
Ackerman Syndrome 
acrocapitofemoral dysplasia  
Acrocephalopolydactylous Dysplasia 
Acromegaloid Features, Overgrowth, Cleft Palate, and Hernia 
Agonadism, XY, with Mental Retardation, Short Stature, Retarded Bone Age, and Multiple Extragenital Malformations 
Al Gazali Khidr Prem Chandran Syndrome 
Al Kaissi Syndrome  
Amaurosis Fugax  
anodontia +   
Aphalangia Syndactyly Microcephaly 
AREDYLD Syndrome 
Auriculoosteodysplasia 
Ayme-Gripp Syndrome  
Bainbridge-Ropers Syndrome  
Bamforth-Lazarus syndrome  
Bellini Chiumello Rimoldi Syndrome 
Berk-Tabatznik Syndrome 
Bhaskar Jagannathan Syndrome 
Bird Headed Dwarfism Montreal Type 
Bjornstad syndrome  
blepharocheilodontic syndrome +   
Blepharophimosis with Ptosis, Syndactyly, and Short Stature 
Book Syndrome 
Borjeson-Forssman-Lehmann syndrome  
Boudhina Yedes Khiari syndrome 
Brachycephaly, Trichomegaly, and Developmental Delay  
brachydactyly type E2  
Brooks-Wisniewski-Brown syndrome 
Cantalamessa Baldini Ambrosi Syndrome 
Cantu Sanchez-Corona Fragoso Syndrome 
Carabelli Anomaly of Maxillary Molar Teeth 
Cataracts, Ataxia, Short Stature, and Mental Retardation 
Catatrichy 
Chitty Hall Baraitser Syndrome 
chromosome 15q26-qter deletion syndrome 
chromosome 17q11.2 deletion syndrome, 1.4Mb  
Chromosome 18 Pericentric Inversion 
Clark-Baraitser Syndrome 
Cleidocranial Dysplasia, Forme Fruste, Dental Anomalies Only  
CODAS Syndrome  
Coffin Syndrome 1 
color blindness +   
Congenital Deafness with Inner Ear Agenesis, Microtia, and Microdontia  
Congenital Deafness, and Onychodystrophy, Autosomal Dominant  
Congenital Woolly Hair +   
Copper Deficiency, Familial Benign 
cortical blindness +   
Cote Katsantoni Syndrome 
COUSIN SYNDROME  
Coxoauricular Syndrome 
Craniofacial Abnormalities, Cataracts, Congenital Heart Disease, Sacral Neural Tube Defects, and Growth and Developmental Retardation 
Craniosynostosis and Dental Anomalies  
Creases, Infra-Auricular Cutaneous, with Tall Stature and Advanced Bone Age 
Crumpled Helices and Small Mouth 
Curatolo Cilio Pessagno Syndrome 
Curly Hair-Ankyloblepharon-Nail Dysplasia Syndrome  
Daish Hardman Lamont Syndrome 
Deaf-Blind Disorders +   
Dens in Dente +  
dental enamel hypoplasia +   
dentin dysplasia +   
dentinogenesis imperfecta +   
Dermoids of Cornea 
Dermoodontodysplasia 
Devriendt syndrome 
Diastema +  
dilated cardiomyopathy with woolly hair and keratoderma +   
Dilated Cardiomyopathy with Woolly Hair, Keratoderma, and Tooth Agenesis  
Distal Renal Tubular Acidosis, with Nephrocalcinosis, Short Stature, Mental Retardation, and Distinctive Facies 
DNA ligase IV deficiency  
Dubowitz syndrome 
Dyschondrosteosis and Nephritis 
Ectodermal Dysplasia 4, Hair/Nail Type  
Ectodermal Dysplasia 9, Hair/Nail Type  
ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME  
Epithelial Squamous Dysplasia, Keratinizing Desquamative, of Urinary Tract 
Euhidrotic Ectodermal Dysplasia 
EVEN-PLUS SYNDROME  
Facial Dysmorphism, Immunodeficiency, Livedo, and Short Stature  
Faciocardiomelic Dysplasia, Lethal 
Fallot Complex with Severe Mental and Growth Retardation 
Familial Osteochondritis Dissecans  
Fetal Growth Retardation +   
Filippi Syndrome  
Floating-Harbor Syndrome  
FLOTCH Syndrome 
folliculitis +   
Forsythe-Wakeling Syndrome 
Frias Syndrome 
Fused Teeth 
Game Friedman Paradice Syndrome 
Gay Feinmesser Cohen Syndrome 
Geleophysic Dysplasia 1  
Geleophysic Dysplasia 2  
Geleophysic Dysplasia 3  
GEMSS Syndrome  
Generalized Lipodystrophy, with Mental Retardation, Deafness, Short Stature, and Slender Bones 
GOMBO Syndrome 
Gomez Lopez Hernandez Syndrome 
Gonadal Dysgenesis, Hypergonadotropic, XX Type, Short Stature, and Recurrent Metabolic Acidosis 
Goniodysgenesis-Mental Retardation-Short Stature Syndrome 
Growth and Developmental Retardation, Ocular Ptosis, Cardiac Defect, and Anal Atresia 
Growth Deficiency and Mental Retardation with Facial Dysmorphism  
Growth Failure, Microcephaly, Mental Retardation, Cataracts, Large Joint Contractures, Osteoporosis, Cortical Dysplasia, and Cerebellar Atrophy 
Growth Mental Deficiency Syndrome of Myhre  
Growth Retardation, Alopecia, Pseudoanodontia and Optic Atrophy  
GROWTH RETARDATION, INTELLECTUAL DEVELOPMENTAL DISORDER, HYPOTONIA, AND HEPATOPATHY  
Growth Retardation, Small and Puffy Hands and Feet, and Eczema 
Grubben de Cock Borghgraef Syndrome 
Hairy Elbows 
Hairy Palms and Soles 
Heme Oxygenase 1 Deficiency  
Hemianopsia 
hereditary spastic paraplegia 9A  
Hersh Podruch Weisskopk Syndrome 
Hirsutism +   
Hooft Disease 
Hunter-McAlpine Syndrome 
Hutterite Cerebroosteonephrodysplasia Syndrome 
hypertrichosis +   
Hypoglossia-Hypodactylia 
hypoparathyroidism-retardation-dysmorphism syndrome  
HYPOTONIA, ATAXIA, DEVELOPMENTAL DELAY, AND TOOTH ENAMEL DEFECT SYNDROME  
hypotrichosis +   
Idiopathic Short Stature, X-Linked  
Insulin-Like Growth Factor I Deficiency  
Insulin-Like Growth Factor I, Resistance To  
Insulin-Like Growth Factor I, Resistance to, due to Increased Binding Protein 
Iridogoniodysgenesis Type 2  
Johanson-Blizzard syndrome  
Jorgenson Lenz Syndrome 
Kaler Garrity Stern Syndrome 
Katsantoni Papadakou Lagoyanni Syndrome 
KBG syndrome  
Kozlowski Rafinski Klicharska Syndrome 
Kozlowski-Krajewska Syndrome 
Kuster Majewski Hammerstein Syndrome 
LADD syndrome  
Ladda Zonana Ramer syndrome 
Langer Mesomelic Dysplasia  
Larsen syndrome  
Larsen Syndrome, Recessive Type  
Laryngotracheal Stenosis, Progressive, with Short Stature and Arthropathy  
Leri-Weill dyschondrosteosis  
Leukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis 
Loucks-Innes Syndrome  
Lowry Maclean syndrome 
Lowry Wood Syndrome 
Macrosomia Adiposa Congenita 
Madelung Deformity 
Malocclusion and Short Stature 
Martinez Monasterio Pinheiro Syndrome 
Megarbane Syndrome 
Meier-Gorlin syndrome +   
Menkes disease +   
Mental and Growth Retardation with Amblyopia 
Mental Retardation Mietens Weber Type 
Mental Retardation with Optic Atrophy, Facial Dysmorphism, Microcephaly, and Short Stature 
Mental Retardation, Microcephaly, Growth Retardation, Joint Contractures, and Facial Dysmorphism 
Mental Retardation, X-Linked, with Short Stature  
Mental Retardation-Hypotonic Facies Syndrome, X-Linked, 1  
Microcephaly Cervical Spine Fusion Anomalies 
Microcephaly Microphthalmos Blindness 
Microcephaly, Growth Deficiency, Seizures, and Brain Malformations  
MICROCEPHALY, GROWTH RESTRICTION, AND INCREASED SISTER CHROMATID EXCHANGE 2  
MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 1   
MICROCEPHALY, SHORT STATURE, AND IMPAIRED GLUCOSE METABOLISM 2  
MICROCEPHALY, SHORT STATURE, AND POLYMICROGYRIA WITH OR WITHOUT SEIZURES  
Microdontia Hypodontia Short Stature 
Milner Khallouf Gibson Syndrome 
Mitochondrial Myopathy with Lactic Acidosis  
Mollica Pavone Antener Syndrome 
monilethrix +   
Morillo-Cucci Passarge Syndrome 
Multiform Ventricular Extrasystoles with Short Stature, Hyperpigmentation and Microcephaly 
Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay 
Nance-Horan syndrome  
Nathalie Syndrome 
Naxos Disease  
Neonatal Zinc Deficiency due to Low Breast Milk Zinc  
NEURODEVELOPMENTAL DISORDER WITH SPASTICITY AND POOR GROWTH  
Neurofaciodigitorenal Syndrome 
Nijmegen Breakage Syndrome-Like Disorder  
Norrie disease  
oculodentodigital dysplasia +   
Oculotrichodysplasia 
Odontodysplasia +   
Odontomicronychial Dysplasia 
Odontotrichoungual-Digital-Palmar Syndrome 
Ogden syndrome  
Omodysplasia Type 1  
Onat Syndrome 
Oroacral Syndrome, Verloes-Koulischer Type 
Osteolysis Syndrome Recessive 
Otodental Dysplasia 
Partington Anderson Syndrome 
Pectus Excavatum, Macrocephaly, Short Stature, Dysplastic Nails 
Pedal Onychogryposis with Keratosis Plantaris and Coarse Hair 
Peters plus syndrome  
Petty Laxova Wiedemann Syndrome 
Pfeiffer Kapferer Syndrome 
Pfeiffer Mayer Syndrome 
Pfeiffer Palm Teller Syndrome 
Photosensitive Trichothiodystrophy 1  
Pili Annulati 
Pili Multigemini 
Pili Torti +  
Pili Torti Developmental Delay Neurological Abnormalities 
Pilotto Syndrome 
Polycystic Kidney, Cataract, and Congenital Blindness 
Polydysspondyly 
Postaxial Polydactyly, with Dental and Vertebral Anomalies 
Premature Aging, Okamoto Type 
Progeria Short Stature Pigmented Nevi 
Progeroid Syndrome, Congenital, Petty Type  
Pseudofolliculitis Barbae  
Pseudomonilethrix 
PSPH deficiency  
Qazi Markouizos syndrome 
Radioulnar Synostosis Retinal Pigment Abnormalities 
Rajab Syndrome  
Ramon Syndrome 
Reardon Wilson Cavanagh Syndrome 
Retinal Aplasia 
Retinal Dystrophy, Juvenile Cataracts, and Short Stature Syndrome  
Rhizomelic Dysplasia, Scoliosis, and Retinitis Pigmentosa 
Rodrigues Blindness 
Rommen Mueller Sybert Syndrome 
Rowley-Rosenberg Syndrome 
Ruijs-Aalfs Syndrome  
Say Meyer Syndrome 
Say Syndrome 
Schaap Taylor Baraitser Syndrome 
Schimke X-Linked Mental Retardation Syndrome 
Scoliosis, Arachnodactyly, and Blindness 
Seemanova Lesny Syndrome 
Severe Combined Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation  
Severe Growth Restriction with Distinctive Facies  
Short Stature Syndrome, Brussels Type 
Short Stature, Facial Dysmorphism, Severe Brachydactyly, and Syndactyly 
Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis  
Short Stature, Optic Nerve Atrophy, and Pelger-Huet Anomaly  
SHORT Syndrome  
Skin Fragility-Woolly Hair Syndrome  
Slavotinek Pike Mills Hurst Syndrome 
Sonoda Syndrome 
Spondyloepimetaphyseal Dysplasia with Abnormal Dentition 
Spondyloepimetaphyseal Dysplasia, Faden-Alkuraya Type  
spondyloepimetaphyseal dysplasia, Pakistani type  
Spondylometaphyseal Dysplasia, 'Corner Fracture' Type  
Stern Lubinsky Durrie Syndrome 
superficial mycosis +  
Supernumerary Tooth +  
syndromic X-linked intellectual disability Cabezas type  
Synostosis of Talus and Calcaneus with Short Stature 
TATTON-BROWN-RAHMAN SYNDROME  
Taurodontism +  
Taurodontism, Microdontia, and Dens Invaginatus 
Teeth Noneruption of with Maxillary Hypoplasia and Genu Valgum 
Teeth, Odd Shapes of 
temtamy preaxial brachydactyly syndrome  
THAUVIN-ROBINET-FAIVRE SYNDROME  
Theodor Hertz Goodman Syndrome 
Thrombocytopenia Robin Sequence 
Thumb Agenesis, Short Stature, and Immunodeficiency 
Thumb, Hypoplastic, with Choroid Coloboma, Poorly Developed Antihelix, and Deafness 
tinea capitis +  
Tonoki Syndrome 
tooth agenesis +   
Tricho-Dento-Osseous Syndrome  
Tricho-Dento-Osseous Syndrome 1 
Trichodysplasia-Xeroderma 
Trichohepatoenteric Syndrome  
Trichohepatoenteric Syndrome 2  
TRICHOMEGALY  
trichorhinophalangeal syndrome type I  
trichorhinophalangeal syndrome type III  
Trichostasis Spinulosa 
Tsukahara Syndrome 
Uncombable Hair Syndrome +   
Vater-Like Defects with Pulmonary Hypertension, Laryngeal Webs, and Growth Deficiency 
Verheij Syndrome  
Vertebral Body Fusion Overgrowth 
Viljoen Kallis Voges Syndrome 
Volcke Soekarman Syndrome 
Wellesley Carmen French Syndrome 
Weyers Acrofacial Dysostosis  
White Forelock with Malformations 
Wiedemann Grosse Dibbern Syndrome 
Winchester Syndrome  
Wittwer Syndrome 
Woolly Hair, Autosomal Recessive +   
Yemenite Deaf-Blind Hypopigmentation Syndrome 
Young Hughes Syndrome 
Zazam Sheriff Phillips Syndrome 
Zerres Rietschel Majewski Syndrome 

Synonyms
Primary IDs: MESH:C535865 ;   RDO:0001206

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