H18.519
BillableEndothelial corneal dystrophy, unspecified eye
Endothelial corneal dystrophy, unspecified eye
Coding Notes
Excludes 2
Conditions not included here, but the patient may have both
- certain conditions originating in the perinatal period (P04-P96)
- certain infectious and parasitic diseases (A00-B99)
- complications of pregnancy, childbirth and the puerperium (O00-O9A)
- congenital malformations, deformations, and chromosomal abnormalities (Q00-Q99)
- diabetes mellitus related eye conditions (E09.3-, E10.3-, E11.3-, E13.3-)
- endocrine, nutritional and metabolic diseases (E00-E88)
- injury (trauma) of eye and orbit (S05.-)
- injury, poisoning and certain other consequences of external causes (S00-T88)
- neoplasms (C00-D49)
- symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
- syphilis related eye disorders (A50.01, A50.3-, A51.43, A52.71)
Also Known As / Clinical Terms
SNOMED CT
- ICE (irido-corneo-endothelial) syndrome129623003
- ICE (iridocorneal endothelial) syndrome129623003
- Irido-corneo-endothelial syndrome129623003
- Iridocorneal endothelial syndrome129623003
- Fuch's endothelial corneal dystrophy193839007
- Fuchs corneal dystrophy193839007
- Fuchs' corneal dystrophy193839007
- Fuchs' endothelial dystrophy193839007
- Iris nodule248510004
- Corneal endothelialitis373425009
- Corneal endotheliitis373425009
- Corneal endotheliolitis373425009
- Chandler syndrome392481002
- Cogan-Reese syndrome404633004
- Iris naevus syndrome404633004
- Iris nevus syndrome404633004
- Nodular unilateral glaucoma404633004
- Corneal endothelial dystrophy416960004
- Dystrophy of corneal endothelium416960004
- Endothelial corneal dystrophy416960004
- CHED II - Congenital hereditary endothelial dystrophy II417395001
- Congenital hereditary endothelial dystrophy type 2417395001
- Congenital hereditary endothelial dystrophy, autosomal recessive form417395001
- CHED-congenital hereditary endothelial dystrophy417651000
- Congenital hereditary endothelial dystrophy417651000
- X-linked endothelial corneal dystrophy718579008
- X-linked endothelial dystrophy of cornea718579008
- Congenital hereditary endothelial dystrophy and perceptive deafness syndrome720749004
- Corneal dystrophy and perceptive deafness syndrome720749004
- Corneal dystrophy with progressive deafness720749004
- Harboyan syndrome720749004
- Autosomal dominant keratoconus with early-onset anterior polar cataract722439009
- EDICT (endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning) syndrome722439009
- EDICT syndrome722439009
- Endothelial dystrophy, iris hypoplasia, congenital cataract, stromal thinning syndrome722439009
- Familial keratoconus with cataract722439009
- Congenital corneal dystrophy1003408005
- Congenital dystrophy of cornea1003408005
- Secondary angle-closure glaucoma due to iridocorneal endothelial syndrome1137633000
- Angle-closure due to iridocorneal endothelial syndrome1286851007
- Secondary angle-closure due to iridocorneal endothelial syndrome1286851007
Frequently Asked Questions
What is the ICD-10 code for endothelial corneal dystrophy, unspecified eye?
The ICD-10-CM code for endothelial corneal dystrophy, unspecified eye is H18.519. The full clinical description is "Endothelial corneal dystrophy, unspecified eye". H18.519 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code H18.519 mean?
ICD-10-CM code H18.519 represents "Endothelial corneal dystrophy, unspecified eye". It is classified under Chapter 7: Diseases of the Eye and Adnexa and is a billable/specific code that can be used on a claim.
Is H18.519 a billable code?
Yes, H18.519 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is H18.519 in?
H18.519 is in Chapter 7: Diseases of the Eye and Adnexa (codes H00-H59).
What SNOMED CT codes does H18.519 map to?
H18.519 maps to 15 SNOMED CT concepts: 1286851007, 722439009, 417395001, 417651000, 392481002, and 10 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for H18.519?
H18.519 is linked to 1 UMLS Concept Unique Identifier: C5384702. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.