modern wellness · Symptom

Abnormality of the eye

🩺 HPO Source

HPO ID

HPO Label

Abnormality of the eye

HPO Definition

Any abnormality of the eye, including location, spacing, and intraocular abnormalities.

🔤 Synonyms (3)

Synonyms

Abnormal eyeAbnormality of the eyeEye disease

🔗 Cross-References (5)

SNOMEDCT_US19416009

SNOMEDCT_US371405004

SNOMEDCT_US371409005

UMLSC0015393

UMLSC0015397

🔼 Broader Terms (1)

HP:0000118Phenotypic abnormality

🏥 Conditions where Abnormality of the eye appears

22 · bridged via HPO ↔ OMIM

syndrome OMIM 610031

Cortical Dysplasia, Complex, With Other Brain Malformations 7

disease OMIM 155600

Cutaneous Melanoma

syndrome OMIM 304730

Dermoids of Cornea

syndrome OMIM 202650

Dysgnathia Complex

disease OMIM 155600

Dysplastic Nevus Syndrome

phenotype OMIM 611694

Dystonia With Cerebellar Atrophy

syndrome OMIM 614931

Ectodermal Dysplasia 9, Hair/Nail Type

freq: 0/3 ev: IEA

disease OMIM 155600

Familial Atypical Mole Melanoma Syndrome

syndrome OMIM 230800

Gaucher Disease, Type 1

syndrome OMIM 607225

Hereditary Spastic Paralysis, Infantile Onset Ascending

syndrome OMIM 242600

Iminoglycinuria

disease OMIM 155600

Melanoma, Cutaneous Malignant, 1

syndrome OMIM 155900

Melkersson-Rosenthal Syndrome

syndrome OMIM 256030

Nemaline Myopathy 2

syndrome OMIM 164185

Ocular Cicatricial Pemphigoid

disease OMIM 202650

syndrome OMIM 184840

Pierre Robin Syndrome With Fetal Chondrodysplasia

freq: 0/3 ev: PCS

syndrome OMIM 176860

Protein C Deficiency, Acquired

syndrome OMIM 224750

Schopf-Schulz-Passarge Syndrome (Disorder)

phenotype OMIM 227240

Skin/Hair/Eye Pigmentation, Variation In, 5 (Disorder)

syndrome OMIM 182290

Smith-Magenis Syndrome

freq: HP:0040282 ev: PCS

syndrome OMIM 176860

Thrombophilia, Hereditary, Due To Protein C Deficiency, Autosomal Dominant