Corneal opacity

Symptom Information:

Symptom ID: HPO:0007957
Synonyms:
Corneal clouding [HPO:0007957]
Reduction of corneal clarity [HPO:0007957]
Corneal opacity (disorder) [Orphanet:4340]
Corneal Opacity [Orphanet:4340]
Corneal clouding [OMIM:Corneal clouding]
Corneal opacity [OMIM:Corneal opacity]
Corneal clouding/opacity/vascularisation [Orphanet:4340]
Corneal opacity [Orphanet:4340]
Corneal opacity [MedDRA:10011035]
Central opacity of cornea [MedDRA:10011035]
Corneal cataract [MedDRA:10011035]
Corneal epithelium opacity [MedDRA:10011035]
Corneal haze [MedDRA:10011035]
Corneal opacity and other disorders of cornea [MedDRA:10011035]
Corneal opacity, unspecified [MedDRA:10011035]
Corneal scars and opacities [MedDRA:10011035]
Minor opacity of cornea [MedDRA:10011035]
Opacity corneal [MedDRA:10011035]
Peripheral opacity of cornea [MedDRA:10011035]
Subepithelial opacities [MedDRA:10011035]
Corneal clouding [MedDRA:10011035]
Macula corneae [MedDRA:10011035]
Crocodile shagreen [MedDRA:10011035]
Corneal clouding (Detroit type 107680.0011, APOA1 deficiency 107680.0014) [OMIM:Corneal clouding (Detroit type 107680.0011, APOA1 deficiency 107680.0014)]
Corneal clouding (in some) [OMIM:Corneal clouding (in some)]
Corneal clouding (rare) [OMIM:Corneal clouding (rare)]
Corneal clouding (variable) [OMIM:Corneal clouding (variable)]
Corneal haze (rare) [OMIM:Corneal haze (rare)]
Corneal opacities [OMIM:Corneal opacities]
Corneal opacity (rare) [OMIM:Corneal opacity (rare)]
Quality:
Cross references:
HPO:0007759 "Opacification of the corneal stroma" [Orphanet:4340]
Orphanet:4340 "Corneal clouding/opacity/vascularisation" [Orphanet:4340]
OMIM: "Corneal clouding" [OMIM:Corneal clouding]
OMIM: "Corneal opacity" [OMIM:Corneal opacity]
OMIM: "Corneal clouding (Detroit type 107680.0011, APOA1 deficiency 107680.0014)" [OMIM:Corneal clouding (Detroit type 107680.0011, APOA1 deficiency 107680.0014)]
OMIM: "Corneal clouding (in some)" [OMIM:Corneal clouding (in some)]
OMIM: "Corneal clouding (rare)" [OMIM:Corneal clouding (rare)]
OMIM: "Corneal clouding (variable)" [OMIM:Corneal clouding (variable)]
OMIM: "Corneal haze (rare)" [OMIM:Corneal haze (rare)]
OMIM: "Corneal opacities" [OMIM:Corneal opacities]
OMIM: "Corneal opacity (rare)" [OMIM:Corneal opacity (rare)]
UMLS:C0010038 "Corneal Opacity" [Orphanet:4340]
Is a (Direct Parents):
Orphanet Abnormality of the eye
HPO         Abnormality of the cornea
MedDRA Corneal structural change, deposit and degeneration
Orphanet Opacification of the corneal stroma
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the eye(HPO:0000478)
          Abnormal eye morphology(HPO:0012372)
             Abnormality of the globe(HPO:0012374)
                Abnormality of the anterior segment of the globe(HPO:0004328)
                   Abnormality of the cornea(HPO:0000481)
                      Corneal opacity(HPO:0007957)
MedDRA:
Eye disorders(MedDRA:10015919)
    Anterior eye structural change, deposit and degeneration(MedDRA:10002693)
       Corneal structural change, deposit and degeneration(MedDRA:10011049)
          Corneal opacity(HPO:0007957)
Database Frequency: 84 / 7739
Resource:

All diseases associated with this symptom:

8q21.11 microdeletion syndrome (Orphanet:284160)
ALDH18A1-related De Barsy syndrome (Orphanet:35664)
AXENFELD-RIEGER SYNDROME, TYPE 2 (OMIM:601499)
Alpha-mannosidosis (Orphanet:61)
Autosomal dominant Larsen syndrome (Orphanet:503)
Autosomal recessive proximal renal tubular acidosis (Orphanet:93607)
BRACHYMESOMELIA-RENAL SYNDROME (OMIM:113470)
BRESEK syndrome (Orphanet:85284)
Brachyolmia type 1, Toledo type (Orphanet:93303)
CARPENTER SYNDROME 1 (OMIM:201000)
CHONDROITIN-6-SULFATURIA, DEFECTIVE CELLULAR IMMUNITY, NEPHROTIC SYNDROME (OMIM:215250)
COCKAYNE SYNDROME A (OMIM:216400)
COCKAYNE SYNDROME B (OMIM:133540)
CONGENITAL CORNEAL OPACITIES, CORNEA GUTTATA, AND CORECTOPIA (OMIM:608484)
CORNEAL DYSTROPHY, POSTERIOR POLYMORPHOUS, 2 (OMIM:609140)
Congenital blindness due to retinal non-attachment (Orphanet:300337)
Congenital hereditary endothelial dystrophy type II (Orphanet:293603)
Congenital intrauterine infection-like syndrome (Orphanet:1229)
Corneal dystrophy - perceptive deafness (Orphanet:1490)
Corneal-cerebellar syndrome (Orphanet:3177)
Cystinosis (Orphanet:213)
Distal monosomy 6p (Orphanet:96125)
EDICT syndrome (Orphanet:293936)
Fabry disease (Orphanet:324)
Familial LCAT deficiency (Orphanet:79293)
Familial ocular anterior segment mesenchymal dysgenesis (Orphanet:88632)
Familial vascular leukoencephalopathy (Orphanet:36383)
Fish-eye disease (Orphanet:79292)
Fraser syndrome (Orphanet:2052)
GLAUCOMA 3, PRIMARY CONGENITAL, D (OMIM:613086)
GM1 gangliosidosis type 3 (Orphanet:79257)
Galactosialidosis (Orphanet:351)
Galloway-Mowat syndrome (Orphanet:2065)
Gaucher disease (Orphanet:355)
Gaucher disease - ophthalmoplegia - cardiovascular calcification (Orphanet:2072)
Gaucher disease type 1 (Orphanet:77259)
Gaucher disease type 2 (Orphanet:77260)
Gaucher disease type 3 (Orphanet:77261)
Gómez-López-Hernández syndrome (Orphanet:1532)
Hereditary mucoepithelial dysplasia (Orphanet:1839)
Hereditary sensory and autonomic neuropathy type 4 (Orphanet:642)
Histiocytoid cardiomyopathy (Orphanet:137675)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 11 (OMIM:602400)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Ichthyosis-hypotrichosis syndrome (Orphanet:91132)
Isolated aniridia (Orphanet:250923)
LCAT deficiency (Orphanet:650)
LETHAL SHORT-LIMB SKELETAL DYSPLASIA, AL GAZALI TYPE (OMIM:601356)
Linear nevus sebaceus syndrome (Orphanet:2612)
MUCOLIPIDOSIS III ALPHA/BETA (OMIM:252600)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 (OMIM:236670)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 3 (OMIM:253280)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 5 (OMIM:613153)
Mandibulofacial dysostosis - macroblepharon - macrostomia (Orphanet:357158)
Mucolipidosis type 4 (Orphanet:578)
Mucopolysaccharidosis type 4 (Orphanet:582)
Mucopolysaccharidosis type 4A (Orphanet:309297)
Mucopolysaccharidosis type 4B (Orphanet:309310)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mucopolysaccharidosis type 7 (Orphanet:584)
Multiple sulfatase deficiency (Orphanet:585)
Muscle-eye-brain disease (Orphanet:588)
Mutilating palmoplantar keratoderma with periorificial keratotic plaques (Orphanet:659)
Norrie disease (Orphanet:649)
Oculodental syndrome, Rutherfurd type (Orphanet:2709)
Oculoosteocutaneous syndrome (Orphanet:2713)
Ophthalmomandibulomelic dysplasia (Orphanet:2741)
PEROXISOME BIOGENESIS DISORDER 1A (ZELLWEGER) (OMIM:214100)
Pelvis-shoulder dysplasia (Orphanet:2839)
Peters anomaly (Orphanet:708)
ROBERTS SYNDROME (OMIM:268300)
SPONDYLOEPIPHYSEAL DYSPLASIA TARDA, X-LINKED (OMIM:313400)
Scheie syndrome (Orphanet:93474)
Schimke immuno-osseous dysplasia (Orphanet:1830)
Schnyder corneal dystrophy (Orphanet:98967)
Stüve-Wiedemann syndrome (Orphanet:3206)
Subaortic stenosis - short stature (Orphanet:3191)
Tangier disease (Orphanet:31150)
Tyrosinemia type 2 (Orphanet:28378)
WINCHESTER SYNDROME (OMIM:277950)
X-linked endothelial corneal dystrophy (Orphanet:293621)
X-linked reticulate pigmentary disorder with systemic manifestations (Orphanet:85453)