2026 ICD-10-CM Diagnosis Code D23.9Other benign neoplasm of skin, unspecified
ICD-10-CM Codes›C00–D49›D10-D36›D23
- Billable — Valid for Submission
- Not Chronic
D23.9 is a billable ICD-10-CM diagnosis code for other benign neoplasm of skin, unspecified. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 606 through 607. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Benign neoplasms.
Code Identity
Code Classification
Approximate SynonymsGuidance
Alternate terms and clinical phrases that map to this code.
- Acantholytic dyskeratotic epidermal nevus
- Acantholytic epidermal nevus
- Achromic nevus
- Acquired angiokeratoma
- Acquired digital fibrokeratoma
- Acral pseudolymphomatous angiokeratoma of children
- Acrosyringeal nevus
- Aneurysmal histiocytoma of skin
- Angiokeratoma circumscriptum
- Angiokeratoma of Mibelli
- Angiokeratoma of skin
- Apocrine adenoma
- Apocrine cystadenoma
- Apocrine hidrocystoma
- Apocrine nevus
- Atrophic dermatofibroma
- Atypical histiocytoma of skin
- Basal cell nevus with comedones
- Benign epithelial neoplasm of skin
- Benign fibrohistiocytic neoplasm of skin
- Benign fibromatous neoplasm of skin
- Benign neoplasm of adnexa of skin
- Benign neoplasm of dermis
- Benign neoplasm of nail apparatus
- Benign neoplasm of sebaceous gland
- Benign neoplasm of skin
- Benign neoplasm of skin with pilar differentiation
- Benign neoplasm of sweat gland
- Benign skin tumor with apocrine differentiation
- Benign skin tumor with eccrine differentiation
- Benign tumor of skin with sebaceous differentiation
- Blue nevus of skin
- Brooke-Spiegler syndrome
- Cellular blue nevus of skin
- Cellular histiocytoma of skin
- Circumscribed storiform collagenoma
- Clear cell acanthoma
- Clear cell histiocytoma of skin
- Clear cell syringoma
- Collagen nevus of skin
- Common blue nevus of skin
- Congenital panfollicular nevus
- Connective tissue nevus of skin
- Cutaneous leiomyoma
- Cutaneous lymphadenoma
- Cutaneous neurofibroma
- Cutaneous neuroma
- Cutaneous papillomatosis
- Cutaneous storiform neurofibroma
- Cystic trichoblastoma
- Dermal nerve sheath myxoma
- Dermal nerve sheath myxoma, cellular
- Dermatofibroma
- Dermatomyofibroma
- Dermoid cyst of skin
- Desmoplastic trichilemmoma
- Desmoplastic trichoepithelioma
- Eccrine angiomatous hamartoma
- Eccrine dermal cylindroma
- Eccrine dermal duct tumor
- Eccrine epithelioma
- Eccrine hidradenoma
- Eccrine hidrocystoma
- Eccrine mixed tumor
- Eccrine nevus
- Eccrine papillary adenoma
- Eccrine poroma
- Eccrine spiradenoma
- Eccrine syringofibroadenoma
- Elastofibroma
- Elastofibroma of skin
- Epidermal nevus
- Epithelioid and spindle cell nevus
- Eruptive collagenoma of skin
- Eruptive syringomata
- Familial cutaneous collagenoma
- Familial multiple cylindroma
- Familial multiple discoid fibroma
- Familial multiple pilomatrixoma
- Familial multiple syringomata
- Familial multiple trichoepitheliomata
- Fat-storing hamartoma of dermal dendrocytes
- Fibrofolliculoma
- Fibrous histiocytoma of skin
- Florid cutaneous papillomatosis
- Ganglioneuroma
- Ganglioneuroma of skin
- Generalized eruptive histiocytoma
- Giant solitary trichoepithelioma
- Granular cell histiocytoma of skin
- Halo nevus
- Hamartoma of apocrine sweat gland apparatus
- Hamartoma of eccrine sweat gland apparatus
- Hamartoma of pilosebaceous apparatus
- Hamartoma of skin
- Hamartoma of skin appendage
- Hereditary leiomyomatosis and renal cell carcinoma
- Hidradenoma
- Hidroacanthoma simplex
- Inflammatory epidermal nevus
- Intraepidermal epithelioma of Jadassohn
- Keloidal histiocytoma of skin
- Large cell acanthoma
- Lichenoid epidermal nevus
- Linear sebaceous nevus sequence
- Lipomatous hamartoma
- Mantleoma
- Mixed tumor of soft tissue
- Moniliform hamartoma
- Multiple agminated spitz nevi
- Multiple dysplastic nevi
- Multiple fibrofolliculomas
- Multiple self-healing epithelioma of Ferguson-Smith
- Multiple stucco keratoses
- Myofibroma
- Myopericytoma
- Myopericytoma of skin
- Neonatal adnexal polyp
- Neuromuscular hamartoma
- Nevus anelasticus
- Nevus elasticus
- Nevus lipomatosus cutaneous superficialis
- Onychocytic matricoma
- Onychomatricoma
- Osteoma cutis
- Palisaded encapsulated neuroma
- Palisaded histiocytoma of skin
- Papillary hidradenoma
- Papilloma of skin
- Perifollicular fibroma
- Pigmented histiocytoma of skin
- Pilar sheath acanthoma
- Pilomatrixoma
- Pleomorphic fibroma
- Porokeratotic eccrine ostial and dermal duct nevus
- Schwannoma of skin
- Sclerosing angioma of skin
- Sebaceoma
- Sebaceous adenoma of skin
- Sebaceous nevus
- Sebaceous trichofolliculoma
- Shagreen patch
- Solitary cutaneous leiomyoma
- Solitary papular angiokeratoma
- Spitz nevus with intraepidermal pagetoid spread
- Squamous cell papilloma of skin
- Storiform collagenoma
- Stucco keratosis
- Syringocystadenoma
- Syringocystadenoma papilliferum
- Syringoma
- Trichilemmoma
- Trichoadenoma
- Trichoblastoma
- Trichodiscoma
- Trichoepithelioma
- Trichofolliculoma
- Trichogerminoma
- Tumor of follicular infundibulum
- Vascular hamartoma of skin
- Vascular hamartomas
- Verruciform xanthoma of skin
- Winer's dilated pore
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
- Adenoma - See Also: Neoplasm, benign, by site;
- apocrine
- unspecified site - D23.9
External Cause of Injuries IndexGuidance
References for this code in the External Cause of Injuries Index.
- Adenoma
- apocrine
- unspecified site
Clinical ClassificationClinical
AHRQ’s CCSR groups this code into broader clinical categories.
Clinical InformationClinical
Myopericytoma
rare myofibroma-like perivascular soft tissue tumor, usually benign, characterized by concentric perivascular proliferation.Ganglioneuroma
a benign neoplasm that usually arises from the sympathetic trunk in the mediastinum. histologic features include spindle cell proliferation (resembling a neurofibroma) and the presence of large ganglion cells. the tumor may present clinically with horner syndrome or diarrhea due to ectopic production of vasoactive intestinal peptide. (from devita et al., cancer: principles and practice of oncology, 5th ed, p966)Myofibroma
a benign tumor that consists chiefly of fibrous connective tissue, with variable numbers of muscle cells forming portions of the neoplasm (from stedman's, 27th ed).Myofibromatosis
a condition characterized by multiple formations of myofibromas (leiomyoma).Pilomatrixoma
a tumor composed of cells resembling those of the hair matrix, which undergo 'mummification' and may calcify. it is a relatively uncommon tumor, which may occur at any age from infancy. the majority of patients are under 20, and females are affected more than males. the lesion is usually a solitary deep dermal or subcutaneous tumor 3-30 mm in diameter, situated in the head, neck, or upper extremity. (from rook et al., textbook of dermatology, 4th ed, p2401)Adenoma, Pleomorphic
a benign, slow-growing tumor, most commonly of the salivary gland, occurring as a small, painless, firm nodule, usually of the parotid gland, but also found in any major or accessory salivary gland anywhere in the oral cavity. it is most often seen in women in the fifth decade. histologically, the tumor presents a variety of cells: cuboidal, columnar, and squamous cells, showing all forms of epithelial growth. (dorland, 27th ed)Syringoma
a benign tumor of the sweat glands which is usually multiple and results from malformation of sweat ducts. it is uncommon and more common in females than in males. it is most likely to appear at adolescence, and further lesions may develop during adult life. it does not appear to be hereditary. (rook et al., textbook of dermatology, 4th ed, pp2407-8)Horner Syndrome
a syndrome associated with defective sympathetic innervation to one side of the face, including the eye. clinical features include miosis; mild blepharoptosis; and hemifacial anhidrosis (decreased sweating)(see hypohidrosis). lesions of the brain stem; cervical spinal cord; first thoracic nerve root; apex of the lung; carotid artery; cavernous sinus; and apex of the orbit may cause this condition. (from miller et al., clinical neuro-ophthalmology, 4th ed, pp500-11)Leiomyoma
a benign tumor derived from smooth muscle tissue, also known as a fibroid tumor. they rarely occur outside of the uterus and the gastrointestinal tract but can occur in the skin and subcutaneous tissue, probably arising from the smooth muscle of small blood vessels in these tissues.Cutaneous Junctional Nevus|Intraepidermal Nevus|Intraepidermal Nevus of Skin|Intraepidermal Nevus of the Skin|Intraepidermal nevus|Junctional Nevus of Skin|Junctional Nevus of the Skin|Junctional Skin Nevus|Skin Junction Nevus|Skin Junctional Melanocytic Nevus|Skin Junctional Nevus|junctional nevus
a cutaneous nevus characterized by the presence of an intraepidermal proliferation of nevus cells. the nevus cells form multiple nests in the dermal-epidermal junction. it presents as a small, slightly raised, pigmented skin lesion.Becker Nevus|Becker's Nevus|Linear Papular Ectodermal-Mesodermal Hamartoma|Melanosis Neviformis|Pigmented Hairy Epidermal Nevus|Pigmented Hairy Nevus of Becker|Progressive Cribriform and Zosteriform Hyperpigmentation
a benign lesion that is sometimes congenital and consists of an overgrowth of the epidermis and the presence of melanin-containing cells. it is found mostly in males and typically develops during childhood or adolescence, becoming darker and more hairy after puberty.Epidermal Nevus
a benign, pigmented skin growth caused by an overgrowth of the epidermis. it is typically seen at birth, but can develop in early childhood or later in life. most cases are sporadic, but familial patterns of inheritance have been observed.Junctional Nevus|Intraepidermal Nevus|Intraepidermal Nevus of Skin|Intraepidermal Nevus of the Skin|Intraepidermal nevus|Junction Nevus|Junction nevus|Junctional Melanocytic Nevus|Junctional Melanocytoma|Junctional Nevus of Skin|Junctional Nevus of the Skin|Junctional Skin Nevus|Junctional nevus, NOS|junctional nevus
a nevus characterized by the presence of an intraepidermal proliferation of nevus cells. the nevus cells form multiple nests in the dermal-epidermal junction. it presents as a small, slightly raised, pigmented skin lesion.Verrucous Nevus|Verrucous Epidermal Nevus
a benign wart-like, pigmented skin lesion appearing on various parts of the body at birth or early in childhood, usually in linear groupings.Trichoadenoma
a rare benign tumor of the hair follicle occurring usually in the face or buttocks.Basal Cell Nevus with Comedones
a type of pilosebaceous hamartoma characterized by basal cell epitheliomata, epidermoid cysts and comedones, and epidermal atrophy.Trichofolliculoma
a skin appendage neoplasm with follicular differentiation. it usually occurs in the head and neck region, particularly the face. it presents as a solitary dome-shaped small lesion. the clinical course is benign.Lipomatosis of Nerve|Fibrolipomatous Hamartoma of Peripheral Nerve|Neural Fibrolipoma|Peripheral Nerve Fibrolipomatous Hamartoma
a tumor composed of mature adipocytes and fibrous tissue infiltrating the epineurium and peripheral nerves. it is often seen at birth or during childhood and may be associated with macrodactyly.Lipomatous Hamartoma
a benign hamartomatous lesion composed predominantly of adipose tissue.Thymolipoma|Thymolipomatous Hamartoma
a well-circumscribed tumor of the thymus composed of islands of normal thymic parenchyma and mature adipose tissue. it is not clear if thymolipoma is a neoplastic or non-neoplastic lesion.Osteoma Cutis
heterotopic ossification of the skin not associated with a preexisting lesion or process, such as inflammation or neoplasia.Progressive Heterotopic Heteroplasia|Osteoma Cutis|Progressive Osseous Heteroplasia
loss of function mutation(s) in the paternal allele of the gnas gene, encoding guanine nucleotide-binding protein g(s) subunit alpha isoforms short resulting in dermal ossification beginning in infancy, followed by increasing and extensive heterotopic bone formation in deep muscle and fascia.Pleomorphic Fibroma
a benign, often polypoid, fibroblastic neoplasm characterized by bizarre pleomorphic cells. (who 2018)Large Cell Acanthoma
a benign, well-circumscribed skin squamous lesion characterized by the presence of enlarged keratinocytes with nuclei twice the normal size. (who 2018)Junctional Nevus|Intraepidermal Nevus|Intraepidermal Nevus of Skin|Intraepidermal Nevus of the Skin|Intraepidermal nevus|Junction Nevus|Junction nevus|Junctional Melanocytic Nevus|Junctional Nevus of Skin|Junctional Nevus of the Skin|Junctional Skin Nevus|Junctional nevus, NOS|junctional nevus
a nevus characterized by the presence of an intraepidermal proliferation of nevus cells. the nevus cells form multiple nests in the dermal-epidermal junction. it presents as a small, slightly raised, pigmented skin lesion.Spindle-Cell Predominant Trichodiscoma|Neurofollicular Hamartoma|SCPT
a trichodiscoma characterized by the presence of abundant mucinous stroma and spindle-cell fibrocytic proliferation.Trichodiscoma
a rare hamartomatous papular lesion that arises from the hair follicle. it shares morphological features with fibrofolliculoma, but in contrast to fibrofolliculoma, the predominant component is stroma.Trichofolliculoma
a hair follicle lesion that presents as a solitary, colored, dome-shaped small papule. it consists of a central cystic follicular infundibulum from which numerous smaller hair follicles emanate into the surrounding dermis. the clinical course is benign.Trichogerminoma
a rare subtype of trichoblastoma characterized by the presence of lobules of basaloid cells. the lobules are separated by fibrous stroma. it is associated with the expression of recurrent foxk1/grhl and gps2/grhl gene fusions.Dermal Nerve Sheath Myxoma
a benign neoplasm with nerve sheath features that arises from the dermis and subcutaneous tissue. it manifests as an asymptomatic nodule and most often arises from the extremities. it is composed of spindle and epithelioid cells in a myxoid stroma.Pleomorphic Fibroma
a benign fibroblastic dermal neoplasm characterized by the presence of bizarre pleomorphic cells. it is associated with rb1 gene deletion and presents with small polyps and papules affecting the extremities, trunk, and head and neck.Pleomorphic Onychomatricoma|Subungual Pleomorphic Fibroma|Unguioblastic Fibroma
an onychomatricoma characterized by the presence of neoplastic fibroepithelial cells with multinucleated and pleomorphic nuclei.Myxoid Onychomatricoma
an onychomatricoma characterized by the presence of myxoid stromal changes.Onychomatricoma
a rare benign neoplasm that arises from the nail matrix and rarely proximal nail fold and is composed of fibroepithelial cells. it is usually located in fingers and less often in toes.Pigmented Onychomatricoma
an onychomatricoma characterized by the presence of epithelial and nail plate melanin pigmentation.Proliferative Onychomatricoma
an onychomatricoma characterized by the presence of marked epithelial proliferation.
Table of NeoplasmsClinical
Anatomical sites in the Table of Neoplasms that reference this code family.
| Site | Malig. Primary | Malig. Secondary | Ca in situ | Benign | Uncertain | Unspec. |
|---|---|---|---|---|---|---|
| connective tissue NEC › skin (dermis) NEC [See Also: Neoplasm, skin, by site] | C44.90 | C79.2 | D04.9 | D23.9 | D48.5 | D49.2 |
| nail [See Also: Neoplasm, skin, limb] | C44.90 | C79.2 | D04.9 | D23.9 | D48.5 | D49.2 |
| scar NEC [See Also: Neoplasm, skin, by site] | C44.90 | C79.2 | D04.9 | D23.9 | D48.5 | D49.2 |
| skin NOS | C44.90 | C79.2 | D04.9 | D23.9 | D48.5 | D49.2 |
| skin NOS › limb NEC | C44.90 | C79.2 | D04.9 | D23.9 | D48.5 | D49.2 |
| skin NOS › specified sites NEC | C44.80 | C79.2 | D04.8 | D23.9 | D48.5 | D49.2 |
| sudoriferous, sudoriparous gland, site unspecified | C44.90 | C79.2 | D04.9 | D23.9 | D48.5 | D49.2 |
| sweat gland (apocrine) (eccrine), site unspecified | C44.90 | C79.2 | D04.9 | D23.9 | D48.5 | D49.2 |
Patient EducationClinical
Benign Tumors
Tumors are abnormal growths in your body. They can be either benign or malignant. Benign tumors aren't cancer. Malignant ones are. Benign tumors grow only in one place. They cannot spread or invade other parts of your body. Even so, they can be dangerous if they press on vital organs, such as your brain.
Read the full article at MedlinePlus
Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.
Convert D23.9 to ICD-9-CMHistory
The closest ICD-9-CM equivalents under the General Equivalence Mappings.
Code HistoryHistory
Questions About D23.9Overview
Is D23.9 (Other benign neoplasms of skin) a billable code?
Yes. This is a billable ICD-10-CM code, specific enough to report other benign neoplasm of skin, unspecified on HIPAA-covered claims from October 1, 2025 through September 30, 2026.
What MS-DRG does D23.9 group to?
When other benign neoplasm of skin, unspecified is the principal diagnosis on an inpatient stay, it groups to MS-DRG 606, 607, with relative weights from 0.9064 to 1.5132 depending on complications. Higher weights mean higher Medicare reimbursement.
What is the ICD-9 equivalent of D23.9?
Under the General Equivalence Mappings, other benign neoplasm of skin, unspecified converts to ICD-9-CM 216.9 (benign neoplasm skin NOS). The mapping is approximate, so confirm the match fits the documentation.
Footnotes
[1] Not chronic - A diagnosis code that does not fit the criteria for chronic condition (duration, ongoing medical treatment, and limitations) is considered not chronic. Some codes designated as not chronic are acute conditions. Other diagnosis codes that indicate a possible chronic condition, but for which the duration of the illness is not specified in the code description (i.e., we do not know the condition has lasted 12 months or longer) also are considered not chronic.
