H18.599
BillableOther hereditary corneal dystrophies, unspecified eye
Other hereditary corneal dystrophies, 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
- Polymorphous corneal dystrophy29504002
- Posterior polymorphous corneal dystrophy29504002
- Crystalline corneal dystrophy39662004
- Schnyder's crystalline corneal dystrophy39662004
- Ring-like corneal dystrophy75663006
- Combined corneal dystrophy193837009
- Crocodile shagreen of cornea231926003
- CDB type I corneal dystrophy231930000
- Reis-Bucklers' corneal dystrophy231930000
- Stromal corneal dystrophy231931001
- Pre-descemet corneal dystrophy231934009
- Pre-descemet's corneal dystrophy231934009
- Dermochondrocorneal dystrophy254150007
- Francois syndrome254150007
- CDB type II-Corneal dystrophy of Bowman's membrane, type II417065002
- Thiel-Behnke corneal dystrophy417065002
- Fleck corneal dystrophy417183007
- Central cloudy dystrophy of Francois419074008
- Francois' cloudy dystrophy of cornea419074008
- Schnyder crystalline cornea dystrophy419395007
- Gelatinous droplike corneal dystrophy419900000
- Lattice corneal dystrophy type III419900000
- Posterior crocodile shagreen422217003
- Posterior crocodile shagreen of cornea422217003
- Congenital stromal corneal dystrophy702359002
- Decorin associated congenital stromal corneal dystrophy702359002
- Dystrophia corneae parenchymatosa congenita702359002
- Grayson Wilbrandt corneal dystrophy717286002
- Grayson Wilbrandt dystrophy of cornea717286002
- Posterior amorphous corneal dystrophy719296002
- Posterior amorphous stromal dystrophy719296002
- Subepithelial mucinous corneal dystrophy723582004
- Congenital corneal dystrophy1003408005
- Congenital dystrophy of cornea1003408005
- Congenital osteodystrophy5731000119108
Frequently Asked Questions
What is the ICD-10 code for other hereditary corneal dystrophies, unspecified eye?
The ICD-10-CM code for other hereditary corneal dystrophies, unspecified eye is H18.599. The full clinical description is "Other hereditary corneal dystrophies, unspecified eye". H18.599 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code H18.599 mean?
ICD-10-CM code H18.599 represents "Other hereditary corneal dystrophies, 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 H18.599 a billable code?
Yes, H18.599 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is H18.599 in?
H18.599 is in Chapter 7: Diseases of the Eye and Adnexa (codes H00-H59).
What SNOMED CT codes does H18.599 map to?
H18.599 maps to 21 SNOMED CT concepts: 419900000, 231930000, 417065002, 419074008, 193837009, and 16 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for H18.599?
H18.599 is linked to 1 UMLS Concept Unique Identifier: C5384722. 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.