Corneal opacity
Symptom Information:
Symptom ID: | HPO:0007957 | ||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |