List of ICD-9 codes 680–709: diseases of the skin and subcutaneous tissue

12. Diseases of the skin and subcutaneous tissue (680–709)

Firmicutes	Staphylococcus Staphylococcal scalded skin syndrome Impetigo Toxic shock syndrome Streptococcus Impetigo Cutaneous group B streptococcal infection Streptococcal intertrigo Cutaneous Streptococcus iniae infection Erysipelas / Chronic recurrent erysipelas Scarlet fever Corynebacterium Erythrasma Listeriosis Clostridium Gas gangrene Dermatitis gangrenosa Mycoplasma Erysipeloid of Rosenbach

Actinobacteria	Mycobacterium-related: Aquarium granuloma Borderline lepromatous leprosy Borderline leprosy Borderline tuberculoid leprosy Buruli ulcer Erythema induratum Histoid leprosy Lepromatous leprosy Leprosy Lichen scrofulosorum Lupus vulgaris Miliary tuberculosis Mycobacterium avium-intracellulare complex infection Mycobacterium haemophilum infection Mycobacterium kansasii infection Papulonecrotic tuberculid Primary inoculation tuberculosis Rapid growing mycobacterium infection Scrofuloderma Tuberculosis cutis orificialis Tuberculosis verrucosa cutis Tuberculous cellulitis Tuberculous gumma Tuberculoid leprosy Cutaneous actinomycosis Nocardiosis Cutaneous diphtheria infection Arcanobacterium haemolyticum infection Group JK corynebacterium sepsis

Gram -ve

Proteobacteria	α: Endemic typhus Epidemic typhus Scrub typhus North Asian tick typhus Queensland tick typhus Flying squirrel typhus Trench fever Bacillary angiomatosis African tick bite fever American tick bite fever Rickettsia aeschlimannii infection Rickettsialpox Rocky Mountain spotted fever Human granulocytotropic anaplasmosis Human monocytotropic ehrlichiosis Flea-borne spotted fever Japanese spotted fever Mediterranean spotted fever Flinders Island spotted fever Verruga peruana Brill–Zinsser disease Brucellosis Cat-scratch disease Oroya fever Ehrlichiosis ewingii infection β: Gonococcemia/Gonorrhea/Primary gonococcal dermatitis Melioidosis Cutaneous Pasteurella hemolytica infection Meningococcemia Glanders Chromobacteriosis infection γ: Pasteurellosis Tularemia Vibrio vulnificus Rhinoscleroma Haemophilus influenzae cellulitis Pseudomonal pyoderma / Pseudomonas hot-foot syndrome / Hot tub folliculitis / Ecthyma gangrenosum / Green nail syndrome Q fever Salmonellosis Shigellosis Plague Granuloma inguinale Chancroid Aeromonas infection ε: Helicobacter cellulitis

Other	Syphilid Syphilis Chancre Yaws Pinta Bejel Chlamydia infection Leptospirosis Rat-bite fever Lyme disease Lymphogranuloma venereum

Unspecified
pathogen

Dermatitis and eczema (L20–L30, 690–693,698)

Atopic dermatitis	Besnier's prurigo

Seborrheic dermatitis	Pityriasis simplex capillitii Cradle cap

Contact dermatitis (allergic, irritant)	plants: Urushiol-induced contact dermatitis African blackwood dermatitis Tulip fingers other: Abietic acid dermatitis Diaper rash Airbag dermatitis Baboon syndrome Contact stomatitis Protein contact dermatitis

Eczema	Autoimmune estrogen dermatitis Autoimmune progesterone dermatitis Breast eczema Ear eczema Eyelid dermatitis Topical steroid addiction Hand eczema Chronic vesiculobullous hand eczema Hyperkeratotic hand dermatitis Autosensitization dermatitis/Id reaction Candidid Dermatophytid Molluscum dermatitis Circumostomy eczema Dyshidrosis Juvenile plantar dermatosis Nummular eczema Nutritional deficiency eczema Sulzberger–Garbe syndrome Xerotic eczema

Pruritus/Itch/ Prurigo	Lichen simplex chronicus/Prurigo nodularis by location: Pruritus ani Pruritus scroti Pruritus vulvae Scalp pruritus Drug-induced pruritus Hydroxyethyl starch-induced pruritus Senile pruritus Aquagenic pruritus Aquadynia Adult blaschkitis due to liver disease Biliary pruritus Cholestatic pruritus Prion pruritus Prurigo pigmentosa Prurigo simplex Puncta pruritica Uremic pruritus

Other	substances taken internally: Bromoderma Fixed drug reaction Nummular dermatitis Pityriasis alba Papuloerythroderma of Ofuji

Radiation-related disorders / Photodermatoses (L55–L59, 692.7)

Ultraviolet/ionizing	Sunburn Phytophotodermatitis Solar urticaria Polymorphous light eruption Benign summer light eruption Juvenile spring eruption Acne aestivalis Hydroa vacciniforme Solar erythema

Nonionizing	Actinic rays: Actinic keratosis Atrophic actinic keratosis Hyperkeratotic actinic keratosis Lichenoid actinic keratosis Pigmented actinic keratosis Actinic cheilitis Actinic granuloma Actinic prurigo Chronic actinic dermatitis Infrared/heat: Erythema ab igne (Kangri ulcer Kairo cancer Kang cancer Peat fire cancer ) Cutis rhomboidalis nuchae Poikiloderma of Civatte

Other	Radiation dermatitis Acute Chronic radiodermatitis) Favre–Racouchot syndrome Photoaging Photosensitivity with HIV infection Phototoxic tar dermatitis

Acantholysis
(epidermis)

Pemphigus

Pemphigus vulgaris: Pemphigus vegetans of Hallopeau of Neumann

Pemphigus foliaceus: Pemphigus erythematosus Endemic pemphigus

Paraneoplastic pemphigus

IgA pemphigus Subcorneal pustular Intraepidermal neutrophilic

Other

Transient acantholytic dermatosis

Pemphigoid
(dermis)

IgG:	Bullous pemphigoid Cicatricial pemphigoid Localised Gestational pemphigoid Pemphigoid nodularis Epidermolysis bullosa acquisita

IgA:	Linear IgA bullous dermatosis Childhood Adult

Other bullous

Dermatitis herpetiformis

In diseases
classified elsewhere

Urticaria and erythema (L50–L54, 695, 708)

Urticaria
(acute/chronic)

Allergic urticaria

Urticarial allergic eruption

Physical urticaria

Cold urticaria Familial Primary cold contact urticaria Secondary cold contact urticaria Reflex cold urticaria

Heat urticaria Localized heat contact urticaria Solar urticaria

Dermatographic urticaria Vibratory angioedema Pressure urticaria Cholinergic urticaria Aquagenic urticaria

Other urticaria

Angioedema

Erythema

Erythema multiforme/ drug eruption	Erythema multiforme minor Erythema multiforme major (Stevens–Johnson syndrome, Toxic epidermal necrolysis) panniculitis (Erythema nodosum) Acute generalized exanthematous pustulosis

Figurate erythema	Erythema annulare centrifugum Erythema marginatum Erythema migrans Erythema gyratum repens

Other erythema	Necrolytic migratory erythema Erythema toxicum Erythroderma Palmar erythema Generalized erythema

Papulosquamous disorders (L40–L45, 696–697)

Psoriasis

Pustular	Generalized pustular psoriasis (Impetigo herpetiformis) Acropustulosis/Pustulosis palmaris et plantaris (Pustular bacterid) Annular pustular psoriasis Localized pustular psoriasis

Other	Guttate psoriasis Psoriatic arthritis Psoriatic erythroderma Drug-induced psoriasis Inverse psoriasis Napkin psoriasis Seborrheic-like psoriasis

Parapsoriasis

Other pityriasis

Other lichenoid

Lichen planus	configuration Annular Linear morphology Hypertrophic Atrophic Bullous Ulcerative Actinic Pigmented site Mucosal Nails Peno-ginival Vulvovaginal overlap synromes with lichen sclerosus with lupus erythematosis other: Hepatitis-associated lichen planus Lichen planus pemphigoides

Other	Lichen nitidus Lichen striatus Lichen ruber moniliformis Gianotti–Crosti syndrome Erythema dyschromicum perstans Idiopathic eruptive macular pigmentation Keratosis lichenoides chronica Kraurosis vulvae Lichen sclerosus Lichenoid dermatitis Lichenoid reaction of graft-versus-host disease

Factitial dermatitis (F45.8+L98.1, 306.3+698.4) and psychiatric and organic nervous system disease / neurodermatitis

F	Body dysmorphic disorder Bromidrosiphobia Delusional parasitosis Dermatothlasia Factitious dermatitis Trichotillomania

G	Complex regional pain syndrome Congenital insensitivity to pain with anhidrosis Meralgia paraesthetica Riley–Day syndrome Sciatic nerve injury Syringomyelia Trigeminal neuralgia

K	Glossodynia

L	Malum perforans pedis Neurotic excoriations Factitial lymphedema

Ungrouped	Atypical chronic pain syndrome Brachioradial pruritus Notalgia paresthetica Postencephalitic trophic ulcer Psychogenic pruritus Scalp dysesthesia Scrotodynia/Vulvodynia Traumatic neuroma Trigeminal trophic lesion

Cutaneous keratosis, ulcer, atrophy, and necrobiosis (L82–L94, 700–701.5)

Epidermal thickening

Necrobiosis/granuloma

Necrobiotic/palisading	Granuloma annulare Perforating Generalized Subcutaneous Granuloma annulare in HIV disease Localized granuloma annulare Patch-type granuloma annulare Necrobiosis lipoidica Annular elastolytic giant cell granuloma Granuloma multiforme Necrobiotic xanthogranuloma Palisaded neutrophilic and granulomatous dermatitis Rheumatoid nodulosis Interstitial granulomatous dermatitis/Interstitial granulomatous drug reaction

Foreign body granuloma	Beryllium granuloma Mercury granuloma Silica granuloma Silicone granuloma Zirconium granuloma Soot tattoo Tattoo Carbon stain

Other/ungrouped	eosinophilic dermatosis Granuloma faciale

Dermis/
localized CTD

Cutaneous lupus erythematosus	chronic: Discoid Panniculitis subacute: Neonatal ungrouped: Chilblain Lupus erythematosus–lichen planus overlap syndrome Tumid Verrucous Rowell's syndrome

Scleroderma/ Morphea	Localized scleroderma Localized morphea Morphea–lichen sclerosus et atrophicus overlap Generalized morphea Atrophoderma of Pasini and Pierini Pansclerotic morphea Morphea profunda Linear scleroderma

Atrophic/ atrophoderma	Lichen sclerosus Anetoderma Schweninger–Buzzi anetoderma Jadassohn–Pellizzari anetoderma Atrophoderma of Pasini and Pierini Acrodermatitis chronica atrophicans Semicircular lipoatrophy Follicular atrophoderma Linear atrophoderma of Moulin

Perforating	Kyrle disease Reactive perforating collagenosis Elastosis perforans serpiginosa Perforating folliculitis Acquired perforating dermatosis

Skin ulcer	Pyoderma gangrenosum

Other	Calcinosis cutis Sclerodactyly Poikiloderma vasculare atrophicans Ainhum/Pseudo-ainhum

Mucinosis/Lichen myxedematosus (L98.5, 701.8)

Localized lichen myxedematosus	Discrete papular lichen myxedematosus Acral persistent papular mucinosis Self-healing papular mucinosis/Self-healing juvenile cutaneous mucinosis Papular mucinosis of infancy Atypical lichen myxedematosus Atypical tuberous myxedema Nodular lichen myxedematosus

Other primary mucinoses	Cutaneous focal mucinosis Cutaneous lupus mucinosis Eccrine mucinosis Alopecia mucinosa Perifollicular mucinosis Stiff skin syndrome Generalized lichen myxedematosus

Secondary mucinoses	Basal-cell carcinoma Granuloma annulare

Disorders of skin appendages (L60–L75, 703–706)

Nail

thickness: Onychogryphosis
Onychauxis

shape: Koilonychia
Nail clubbing

behavior: Onychotillomania
Onychophagia

other: Ingrown nail
Anonychia

Hair

Hair loss/
Baldness

noncicatricial alopecia: Alopecia
- areata
- totalis
- universalis
- Ophiasis

Androgenic alopecia (male-pattern baldness)
Hypotrichosis
Telogen effluvium
Traction alopecia
Lichen planopilaris
Trichorrhexis nodosa
Alopecia neoplastica
Anagen effluvium
Alopecia mucinosa

Hypertrichosis

Acneiform eruption

Acne	Acne vulgaris Acne conglobata Acne miliaris necrotica Tropical acne Infantile acne/Neonatal acne Excoriated acne Acne fulminans Acne medicamentosa (e.g., steroid acne) Halogen acne Iododerma Bromoderma Chloracne Oil acne Tar acne Acne cosmetica Occupational acne Acne aestivalis Acne keloidalis nuchae Acne mechanica Acne with facial edema Pomade acne Acne necrotica Blackhead Lupus miliaris disseminatus faciei

Rosacea	Perioral dermatitis Granulomatous perioral dermatitis Phymatous rosacea Rhinophyma Blepharophyma Gnathophyma Metophyma Otophyma Papulopustular rosacea Lupoid rosacea Erythrotelangiectatic rosacea Glandular rosacea Gram-negative rosacea Steroid rosacea Ocular rosacea Persistent edema of rosacea Rosacea conglobata variants Periorificial dermatitis Pyoderma faciale

Ungrouped	Granulomatous facial dermatitis Idiopathic facial aseptic granuloma Periorbital dermatitis SAPHO syndrome

Follicular cysts

"Sebaceous cyst"
- Epidermoid cyst
- Trichilemmal cyst
Steatocystoma
- simplex
- multiplex
Milia

Inflammation

Hidradenitis

Ungrouped

Sweat glands

Eccrine	Miliaria Colloid milium Miliaria crystalline Miliaria profunda Miliaria pustulosa Miliaria rubra Occlusion miliaria Postmiliarial hypohidrosis Granulosis rubra nasi Ross’ syndrome Anhidrosis Hyperhidrosis Generalized Gustatory Palmoplantar

Apocrine	Body odor Chromhidrosis Fox–Fordyce disease

Sebaceous	Sebaceous hyperplasia

Pigmentation disorders/Dyschromia (L80–L81, 709.0)

Hypo-/
leucism

Loss of
melanocytes

Vitiligo	Quadrichrome vitiligo Vitiligo ponctué

Syndromic	Alezzandrini syndrome Vogt–Koyanagi–Harada syndrome

Melanocyte development	Piebaldism Waardenburg syndrome Tietz syndrome

Loss of melanin/
amelanism

Albinism	Oculocutaneous albinism Ocular albinism

Melanosome transfer	Hermansky–Pudlak syndrome Chédiak–Higashi syndrome Griscelli syndrome Elejalde syndrome Griscelli syndrome type 2 Griscelli syndrome type 3

Other	Cross syndrome ABCD syndrome Albinism–deafness syndrome Idiopathic guttate hypomelanosis Phylloid hypomelanosis Progressive macular hypomelanosis

Leukoderma w/o
hypomelanosis

Ungrouped

Hyper-

Melanin/
Melanosis/
Melanism

Reticulated	Dermatopathia pigmentosa reticularis Pigmentatio reticularis faciei et colli Reticulate acropigmentation of Kitamura Reticular pigmented anomaly of the flexures Naegeli–Franceschetti–Jadassohn syndrome Dyskeratosis congenita X-linked reticulate pigmentary disorder Galli–Galli disease Revesz syndrome

Diffuse/ circumscribed	Lentigo/Lentiginosis: Lentigo simplex Liver spot Centrofacial lentiginosis Generalized lentiginosis Inherited patterned lentiginosis in black persons Ink spot lentigo Lentigo maligna Mucosal lentigines Partial unilateral lentiginosis PUVA lentigines Melasma Erythema dyschromicum perstans Lichen planus pigmentosus Café au lait spot Poikiloderma (Poikiloderma of Civatte Poikiloderma vasculare atrophicans) Riehl melanosis

Linear	Incontinentia pigmenti Scratch dermatitis Shiitake mushroom dermatitis

Other/ ungrouped	Acanthosis nigricans Freckle Familial progressive hyperpigmentation Pallister–Killian syndrome Periorbital hyperpigmentation Photoleukomelanodermatitis of Kobori Postinflammatory hyperpigmentation Transient neonatal pustular melanosis

Other
pigments

Iron	Hemochromatosis Iron metallic discoloration Pigmented purpuric dermatosis Schamberg disease Majocchi's disease Gougerot–Blum syndrome Doucas and Kapetanakis pigmented purpura/Eczematid-like purpura of Doucas and Kapetanakis Lichen aureus Angioma serpiginosum Hemosiderin hyperpigmentation

Other metals	Argyria Chrysiasis Arsenic poisoning Lead poisoning Titanium metallic discoloration

Other	Carotenosis Tattoo Tar melanosis

Dyschromia

Cutaneous vasculitis and other vascular-related cutaneous conditions (L95, 709.1)

Cutaneous vasculitis	Erythema elevatum diutinum Capillaritis Urticarial vasculitis Nodular vasculitis

Microvascular occlusion	Calciphylaxis Cryoglobulinemic purpura/Cryoglobulinemic vasculitis vascular coagulopathy: Livedoid vasculitis Livedoid dermatitis Perinatal gangrene of the buttock Malignant atrophic papulosis Sneddon's syndrome

Purpura	Nonthrombocytopenic purpura: Cryofibrinogenemic purpura Drug-induced purpura Food-induced purpura IgA vasculitis Obstructive purpura Orthostatic purpura Purpura fulminans Purpura secondary to clotting disorders Purpuric agave dermatitis Pigmentary purpuric eruptions Solar purpura Traumatic purpura Waldenström hyperglobulinemic purpura Painful bruising syndrome ungrouped: Paroxysmal hand hematoma Postcardiotomy syndrome Deep vein thrombosis Superficial thrombophlebitis Mondor's disease Blueberry muffin baby Fibrinolysis syndrome

Systemic vasculitis	see Template:Systemic vasculitis

Vascular malformations	Arteriovenous malformation Bonnet–Dechaume–Blanc syndrome Cobb syndrome Parkes Weber syndrome Sinusoidal hemangioma lymphatic malformation Hennekam syndrome Aagenaes syndrome telangiectasia: Generalized essential telangiectasia Hereditary hemorrhagic telangiectasia Unilateral nevoid telangiectasia

Ulcer	Venous ulcer Arterial insufficiency ulcer Hematopoietic ulcer Neuropathic ulcer Acroangiodermatitis

Lymphedema	see Template:Lymphatic vessel disease

Ungrouped vascular-related cutaneous conditions	Raynaud's phenomenon Thromboangiitis obliterans Erythromelalgia Septic thrombophlebitis Arteriosclerosis obliterans Bier spots/Marshall–White syndrome Cholesterol embolus Reactive angioendotheliomatosis Trousseau's syndrome

List of ICD-9 codes 680–709: diseases of the skin and subcutaneous tissue

12. Diseases of the skin and subcutaneous tissue (680–709)

Infections of skin and subcutaneous tissue (680–686)

Other inflammatory conditions of skin and subcutaneous tissue (690–698)

Other diseases of skin and subcutaneous tissue (700–709)

See also