Abnormality of the cornea

Symptom Information:

Symptom ID: HPO:0000481
Synonyms:
Corneal abnormalities [HPO:0000481]
Corneal abnormality [HPO:0000481]
Cornela disease [HPO:0000481]
Corneal abnormalities [OMIM:Corneal abnormalities]
Quality:
Cross references:
OMIM: "Corneal abnormalities" [OMIM:Corneal abnormalities]
Is a (Direct Parents):
HPO         Abnormality of the anterior segment of the globe
HPO         Abnormality of corneal shape
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)
MedDRA:
Database Frequency: 124 / 7739
Resource:

All diseases associated with this symptom:

3q29 microduplication (Orphanet:251038)
8q21.11 microdeletion syndrome (Orphanet:284160)
Ablepharon macrostomia syndrome (Orphanet:920)
Acrodermatitis enteropathica, zinc deficiency type (Orphanet:37)
Alpha-N-acetylgalactosaminidase deficiency type 2 (Orphanet:79280)
Alpha-mannosidosis (Orphanet:61)
Aniridia (Orphanet:77)
Aniridia - ptosis - intellectual deficit - familial obesity (Orphanet:1067)
Aniridia - renal agenesis - psychomotor retardation (Orphanet:1064)
Apert syndrome (Orphanet:87)
Autoimmune polyendocrinopathy type 1 (Orphanet:3453)
Bartsocas-Papas syndrome (Orphanet:1234)
Bilateral striopallidodentate calcinosis (Orphanet:1980)
Brachyolmia type 1, Toledo type (Orphanet:93303)
Brittle cornea syndrome (Orphanet:90354)
CILIARY DYSKINESIA, PRIMARY, 1 (OMIM:244400)
Cataract-microcornea syndrome (Orphanet:1377)
Cogan syndrome (Orphanet:1467)
Congenital non-bullous ichthyosiform erythroderma (Orphanet:79394)
Congenital rubella syndrome (Orphanet:290)
Corneal dystrophy - perceptive deafness (Orphanet:1490)
Corneal-cerebellar syndrome (Orphanet:3177)
De Barsy syndrome (Orphanet:2962)
Distal monosomy 6p (Orphanet:96125)
Dyschondrosteosis - nephritis (Orphanet:1765)
Dystrophic epidermolysis bullosa (Orphanet:303)
EEC syndrome (Orphanet:1896)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Erythrokeratodermia variabilis (Orphanet:317)
Fabry disease (Orphanet:324)
Familial dysautonomia (Orphanet:1764)
Farber lipogranulomatosis (Orphanet:333)
Focal dermal hypoplasia (Orphanet:2092)
Fryns syndrome (Orphanet:2059)
Fucosidosis (Orphanet:349)
GM1 gangliosidosis (Orphanet:354)
Galactosialidosis (Orphanet:351)
Gaucher disease (Orphanet:355)
Generalized dominant dystrophic epidermolysis bullosa (Orphanet:231568)
Gómez-López-Hernández syndrome (Orphanet:1532)
Hereditary acrokeratotic poikiloderma, Weary type (Orphanet:2907)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypoalphalipoproteinemia (Orphanet:31153)
Ichthyosis follicularis - alopecia - photophobia (Orphanet:2273)
Incontinentia pigmenti (Orphanet:464)
Inherited epidermolysis bullosa (Orphanet:79361)
Isolated aniridia (Orphanet:250923)
Ito hypomelanosis (Orphanet:435)
Junctional epidermolysis bullosa (Orphanet:305)
Junctional epidermolysis bullosa, non-Herlitz type (Orphanet:89840)
KID syndrome (Orphanet:477)
Keratosis follicularis spinulosa decalvans (Orphanet:2340)
Kindler syndrome (Orphanet:2908)
LOC syndrome (Orphanet:2407)
Lacrimo-auriculo-dento-digital syndrome (Orphanet:2363)
Larsen-like osseous dysplasia - short stature (Orphanet:2370)
Lathosterolosis (Orphanet:46059)
Linear verrucous nevus syndrome (Orphanet:2611)
Lowry-MacLean syndrome (Orphanet:2409)
Lyell syndrome (Orphanet:537)
Lymphedema - distichiasis (Orphanet:33001)
Macrosomia - microphthalmia - cleft palate (Orphanet:2432)
Microphthalmia with linear skin defects syndrome (Orphanet:2556)
Mietens syndrome (Orphanet:2557)
Moebius syndrome (Orphanet:570)
Mosaic trisomy 8 (Orphanet:96061)
Mosaic trisomy 9 (Orphanet:99776)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Mucolipidosis type 2 (Orphanet:576)
Mucolipidosis type 3 (Orphanet:577)
Mucolipidosis type 4 (Orphanet:578)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 3 (Orphanet:581)
Mucopolysaccharidosis type 4 (Orphanet:582)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mucopolysaccharidosis type 7 (Orphanet:584)
Mucous membrane pemphigoid (Orphanet:46486)
Multiple non-ossifying fibromatosis (Orphanet:2029)
Multiple sulfatase deficiency (Orphanet:585)
Nasopalpebral lipoma - coloboma - telecanthus (Orphanet:2399)
Neurofibromatosis type 2 (Orphanet:637)
Neutral lipid storage disease (Orphanet:165)
Norrie disease (Orphanet:649)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Oculocerebrorenal syndrome (Orphanet:534)
Oculodental syndrome, Rutherfurd type (Orphanet:2709)
Oculomaxillofacial dysostosis (Orphanet:1794)
Ophthalmomandibulomelic dysplasia (Orphanet:2741)
Osteogenesis imperfecta (Orphanet:666)
Pelvis-shoulder dysplasia (Orphanet:2839)
Peters anomaly (Orphanet:708)
Peters-plus syndrome (Orphanet:709)
Pterygium of the conjunctiva, familial form (Orphanet:2989)
Recessive X-linked ichthyosis (Orphanet:461)
Recessive dystrophic epidermolysis bullosa inversa (Orphanet:79409)
Recessive dystrophic epidermolysis bullosa-generalized other (Orphanet:89842)
Ring dermoid of cornea (Orphanet:91481)
Robinow-like syndrome (Orphanet:3105)
Rothmund-Thomson syndrome (Orphanet:2909)
Rubinstein-Taybi syndrome due to CREBBP mutations (Orphanet:353277)
SHORT syndrome (Orphanet:3163)
Sanjad-Sakati syndrome (Orphanet:2323)
Scheie syndrome (Orphanet:93474)
Schinzel-Giedion syndrome (Orphanet:798)
Severe generalized recessive dystrophic epidermolysis bullosa (Orphanet:79408)
Sialidosis type 1 (Orphanet:812)
Sialidosis type 2 (Orphanet:87876)
Sjögren-Larsson syndrome (Orphanet:816)
Spastic paraparesis - deafness (Orphanet:2815)
Stevens-Johnson syndrome (Orphanet:36426)
Stickler syndrome type 2 (Orphanet:90654)
Syndromic X-linked ichthyosis (Orphanet:281090)
Torg-Winchester syndrome (Orphanet:3460)
Uveal coloboma - cleft lip and palate - intellectual deficit (Orphanet:1473)
Walker-Warburg syndrome (Orphanet:899)
Williams syndrome (Orphanet:904)
X-linked corneal dermoid (Orphanet:1661)
Xeroderma pigmentosum (Orphanet:910)
Xp22.3 microdeletion syndrome (Orphanet:1643)
Yunis-Varon syndrome (Orphanet:3472)
Zellweger syndrome (Orphanet:912)
Zunich-Kaye syndrome (Orphanet:3474)