Dermatology conditions, page 1 of 3
20 conditions on this page, alphabetically from Acne to Eyelid disease. Each entry below describes the condition in full.
On this page
Acne
Overview. A sebaceous gland disease characterized by areas of blackheads, whiteheads, pimples, greasy skin, and possibly scarring. Weyland-Yutani Health System offers diagnosis and ongoing care for acne.
Also known as
- Acne varioliformis
- acne vulgaris
- frontalis acne
Classification
Ontology identifier: DOID:6543 (Human Disease Ontology).
Classification path: disease of anatomical entity › integumentary system disease › skin disease › sebaceous gland disease.
Specialty: Dermatology
Broader conditions
Medical codes
- ICD-10-CM: L70
- ICD-10-CM: L70.2
- ICD-9-CM: 706.0
- MeSH: D000152
- OMIM: 604324
- SNOMED CT: 11381005
- SNOMED CT: 201210008
Care at Weyland-Yutani Health System
Treatment of acne begins with an evaluation in Dermatology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about acne. Bring a list of current medications and any previous test results.
Reference links
Allergic urticaria
allergic urticaria: An urticaria that is characterized by erythematous papules and plaques, has_symptom pruritis, and has_material_basis_in allergic reaction.
Classification
Ontology identifier: DOID:10612 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › allergic disease.
Specialty: Dermatology
Broader conditions
Medical codes
- ICD-10-CM: L50.0
- ICD-9-CM: 708.0
- SNOMED CT: 201260002
Care at Weyland-Yutani Health System
Dermatology specialists lead care for allergic urticaria. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about allergic urticaria. Bring a list of current medications and any previous test results.
Reference links
Angioedema
A skin disease characterized by one or more areas of well-demarcated, non-pitting edema of deep subcutaneous tissues. This page summarizes how angioedema is classified and the care available at Weyland-Yutani Health System.
Also known as
- angioneurotic edema
- Angioneurotic oedema
- giant urticaria
- Quincke's edema
Classification
Ontology identifier: DOID:1558 (Human Disease Ontology).
Classification path: disease of anatomical entity › integumentary system disease › skin disease.
Specialty: Dermatology
Broader conditions
Medical codes
- ICD-10-CM: T78.3
- MeSH: D000799
- SNOMED CT: 41291007
Care at Weyland-Yutani Health System
Dermatology specialists lead care for angioedema. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
If you or a family member may have angioedema, contact your primary care provider or schedule a visit with Dermatology.
Reference links
Angular blepharoconjunctivitis
A blepharoconjunctivitis that is characterized by fissuring, scaling, maceration and erythema of the lateral or medial canthal area. Patients with angular blepharoconjunctivitis are cared for through our Dermatology service line.
Classification
Ontology identifier: DOID:2455 (Human Disease Ontology).
Classification path: disease of anatomical entity › integumentary system disease › skin disease › eyelid disease › blepharitis › blepharoconjunctivitis.
Specialty: Dermatology
Broader conditions
Medical codes
- ICD-10-CM: H10.52
- ICD-9-CM: 372.21
- SNOMED CT: 193871000
Care at Weyland-Yutani Health System
Care for angular blepharoconjunctivitis is coordinated through Dermatology. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about angular blepharoconjunctivitis. Bring a list of current medications and any previous test results.
Reference links
Anhidrosis
A hypohidrosis that is characterized by the inability to sweat and has_symptom hyperthermia and dry skin. Our Dermatology team evaluates and manages anhidrosis.
Also known as
- absence of sweating
- Adiaphoresis
Classification
Ontology identifier: DOID:11156 (Human Disease Ontology).
Classification path: disease of anatomical entity › integumentary system disease › skin disease › sweat gland disease › hypohidrosis.
Specialty: Dermatology
Broader conditions
Medical codes
- ICD-10-CM: L74.4
- ICD-9-CM: 705.0
- MeSH: D007007
- OMIM: 206600
- SNOMED CT: 201189007
Care at Weyland-Yutani Health System
Dermatology specialists lead care for anhidrosis. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
If you or a family member may have anhidrosis, contact your primary care provider or schedule a visit with Dermatology.
Reference links
Atopic dermatitis
Overview. An allergic contact dermatitis that is a chronically relapsing inflammatory allergic response located_in the skin that causes itching and flaking. Weyland-Yutani Health System offers diagnosis and ongoing care for atopic dermatitis.
Also known as
- allergic dermatitis
- atopic eczema
- Atopic neurodermatitis
- Besnier's prurigo
Classification
Ontology identifier: DOID:3310 (Human Disease Ontology).
Classification path: disease of anatomical entity › immune system disease › allergic disease › allergic contact dermatitis.
Specialty: Dermatology
Broader conditions
Medical codes
- ICD-10-CM: L20
- MeSH: D003876
- OMIM: 603165
- OMIM: PS603165
- SNOMED CT: 156331003
Care at Weyland-Yutani Health System
Care for atopic dermatitis is coordinated through Dermatology. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
When to seek care
If you or a family member may have atopic dermatitis, contact your primary care provider or schedule a visit with Dermatology.
Reference links
Autosomal dominant cutis laxa
Overview. A cutis laxa characterized by autosomal dominant inheritance of skin that is loose, hanging, wrinkled and lacking in elasticity. Weyland-Yutani Health System offers diagnosis and ongoing care for autosomal dominant cutis laxa.
Also known as
Classification
Ontology identifier: DOID:0070142 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal dominant disease.
Specialty: Dermatology
Broader conditions
Medical codes
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, autosomal dominant cutis laxa is managed by Dermatology with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
If you or a family member may have autosomal dominant cutis laxa, contact your primary care provider or schedule a visit with Dermatology.
Reference links
Autosomal recessive cutis laxa type I
Overview. A cutis laxa characterized by wrinkled, redundant and sagging inelastic skin and severe systemic manifestations particularly in the lungs, vasculature, and gastrointestinal and genitourinary systems. Weyland-Yutani Health System offers diagnosis and ongoing care for autosomal recessive cutis laxa type I.
Also known as
- autosomal recessive cutis laxa type 1
Classification
Ontology identifier: DOID:0070144 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Dermatology
Broader conditions
More specific conditions
Medical codes
- MeSH: C562628
- SNOMED CT: 254222002
Care at Weyland-Yutani Health System
Dermatology specialists lead care for autosomal recessive cutis laxa type I. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
When to seek care
Questions about autosomal recessive cutis laxa type I? Call your nearest Weyland-Yutani location and ask for Dermatology.
Reference links
Autosomal recessive cutis laxa type IA
Overview. An autosomal recessive cutis laxa type I that has_material_basis_in homozygous or compound heterozygous mutation in the FBLN5 gene on chromosome 14q32. Weyland-Yutani Health System offers diagnosis and ongoing care for autosomal recessive cutis laxa type IA.
Also known as
Classification
Ontology identifier: DOID:0070135 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease › autosomal recessive cutis laxa type I.
Specialty: Dermatology
Broader conditions
Medical codes
- ICD-10-CM: Q82.8
- OMIM: 219100
Care at Weyland-Yutani Health System
Dermatology specialists lead care for autosomal recessive cutis laxa type IA. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
If you or a family member may have autosomal recessive cutis laxa type IA, contact your primary care provider or schedule a visit with Dermatology.
Reference links
Autosomal recessive cutis laxa type II classic type
autosomal recessive cutis laxa type II classic type: A cutis laxa characterized by generalized skin wrinkling, sparse subcutaneous fat, dysmorphic progeroid facial features and severe hypotonia.
Also known as
- ARCL2, classic type
- ARCL2, Debre type
Classification
Ontology identifier: DOID:0070141 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease.
Specialty: Dermatology
Broader conditions
More specific conditions
Medical codes
Care at Weyland-Yutani Health System
Treatment of autosomal recessive cutis laxa type II classic type begins with an evaluation in Dermatology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about autosomal recessive cutis laxa type II classic type. Bring a list of current medications and any previous test results.
Reference links
Autosomal recessive cutis laxa type IIA
autosomal recessive cutis laxa type IIA: An autosomal recessive cutis laxa type II classic type that has_material_basis_in homozygous or compound heterozygous mutations in the ATP6V0A2 gene on chromosome 12q24.
Also known as
Classification
Ontology identifier: DOID:0070134 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease › autosomal recessive cutis laxa type II classic type.
Specialty: Dermatology
Broader conditions
Medical codes
- ICD-10-CM: Q82.8
- OMIM: 219200
Care at Weyland-Yutani Health System
Care for autosomal recessive cutis laxa type IIA is coordinated through Dermatology. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about autosomal recessive cutis laxa type IIA. Bring a list of current medications and any previous test results.
Reference links
Autosomal recessive cutis laxa type IIC
In clinical terms, autosomal recessive cutis laxa type IIC is described as follows: an autosomal recessive cutis laxa type II classic type characterized by cardiovascular involvement that has_material_basis_in homozygous mutation in the ATP6V1E1 gene on chromosome 22q11.
Classification
Ontology identifier: DOID:0070140 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease › autosomal recessive cutis laxa type II classic type.
Specialty: Dermatology
Broader conditions
Medical codes
- ICD-10-CM: Q82.8
- OMIM: 617402
Care at Weyland-Yutani Health System
Care for autosomal recessive cutis laxa type IIC is coordinated through Dermatology. Your clinician will recommend tests and treatments based on your history and symptoms.
Treatment options
Diagnostic tests
When to seek care
If you or a family member may have autosomal recessive cutis laxa type IIC, contact your primary care provider or schedule a visit with Dermatology.
Reference links
Autosomal recessive cutis laxa type IID
An autosomal recessive cutis laxa type II classic type that is characterized by generalized skin wrinkling with sparse subcutaneous fat and dysmorphic progeroid facial featuret and that has_material_basis_in homozygous mutation in the ATP6V1A gene on chromosome 3q13. Our Dermatology team evaluates and manages autosomal recessive cutis laxa type IID.
Also known as
Classification
Ontology identifier: DOID:0070129 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease › autosomal genetic disease › autosomal recessive disease › autosomal recessive cutis laxa type II classic type.
Specialty: Dermatology
Broader conditions
Medical codes
- ICD-10-CM: Q82.8
- OMIM: 617403
Care at Weyland-Yutani Health System
Treatment of autosomal recessive cutis laxa type IID begins with an evaluation in Dermatology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about autosomal recessive cutis laxa type IID. Bring a list of current medications and any previous test results.
Reference links
Blepharitis
An eyelid disease that is characterized by often chronic inflammation of the eyelid, generally the part where eyelashes grow. Our Dermatology team evaluates and manages blepharitis.
Classification
Ontology identifier: DOID:9423 (Human Disease Ontology).
Classification path: disease of anatomical entity › integumentary system disease › skin disease › eyelid disease.
Specialty: Dermatology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: H01.0
- ICD-9-CM: 373.0
- ICD-9-CM: 373.4
- MeSH: D001762
- SNOMED CT: 193907001
- SNOMED CT: 193920003
Care at Weyland-Yutani Health System
Treatment of blepharitis begins with an evaluation in Dermatology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
When to seek care
Questions about blepharitis? Call your nearest Weyland-Yutani location and ask for Dermatology.
Reference links
Cutis laxa
In clinical terms, cutis laxa is described as follows: A skin disease characterized by loose, hanging, wrinkled skin lacking in elasticity.
Also known as
Classification
Ontology identifier: DOID:3144 (Human Disease Ontology).
Classification path: disease of anatomical entity › integumentary system disease › skin disease.
Specialty: Dermatology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: Q82.8
- MeSH: D003483
- OMIM: PS123700
- SNOMED CT: 238825007
Care at Weyland-Yutani Health System
Dermatology specialists lead care for cutis laxa. Plans are tailored to each patient and reviewed regularly.
Treatment options
Diagnostic tests
Related articles
When to seek care
Seek a medical evaluation if you are concerned about cutis laxa. Bring a list of current medications and any previous test results.
Reference links
Dermatitis
In clinical terms, dermatitis is described as follows: A skin disease characterized by itchy, erythematous, vesicular, weeping and crusting patches of skin.
Also known as
Classification
Ontology identifier: DOID:2723 (Human Disease Ontology).
Classification path: disease of anatomical entity › integumentary system disease › skin disease.
Specialty: Dermatology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: L30.9
- MeSH: D003872
- SNOMED CT: 238538009
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, dermatitis is managed by Dermatology with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
Related articles
When to seek care
Seek a medical evaluation if you are concerned about dermatitis. Bring a list of current medications and any previous test results.
Reference links
Dermatographia
A physical urticaria induced by stroking of the skin. Patients with dermatographia are cared for through our Dermatology service line.
Also known as
- dermatographic urticaria
- dermographism
Classification
Ontology identifier: DOID:743 (Human Disease Ontology).
Classification path: disease of anatomical entity › integumentary system disease › skin disease › urticaria › physical urticaria.
Specialty: Dermatology
Broader conditions
Medical codes
- ICD-10-CM: L50.3
- ICD-9-CM: 708.3
- OMIM: 125635
- SNOMED CT: 201263000
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, dermatographia is managed by Dermatology with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
Related articles
When to seek care
If you or a family member may have dermatographia, contact your primary care provider or schedule a visit with Dermatology.
Reference links
Dowling-Degos disease
In clinical terms, Dowling-Degos disease is described as follows: A pigmentation disease characterized by a reticulate pattern of abnormally dark skin coloring, particularly in the body's folds and creases.
Also known as
- dark dot disease
- reticular pigment anomaly of flexures
Classification
Ontology identifier: DOID:0060256 (Human Disease Ontology).
Classification path: disease of anatomical entity › integumentary system disease › skin disease › pigmentation disease.
Specialty: Dermatology
Broader conditions
Medical codes
- MeSH: C562924
- OMIM: 179850
- OMIM: 615327
- OMIM: 615674
- OMIM: 615696
- SNOMED CT: 239133004
Care at Weyland-Yutani Health System
Treatment of Dowling-Degos disease begins with an evaluation in Dermatology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about Dowling-Degos disease? Call your nearest Weyland-Yutani location and ask for Dermatology.
Reference links
Erythrokeratodermia variabilis
erythrokeratodermia variabilis: A skin disease that is characterized by areas of sharply demarcated, brown hyperkeratosis and has_material_basis_in mutations in genes encoding for connexin channels proteins in the epidermis.
Also known as
- Erythrokeratodermia Figurata Variabilis
- Greither Disease
Classification
Ontology identifier: DOID:0050467 (Human Disease Ontology).
Classification path: genetic disease › monogenic disease.
Specialty: Dermatology
Broader conditions
Medical codes
- MeSH: D056266
- OMIM: PS133200
- SNOMED CT: 70041004
Care at Weyland-Yutani Health System
Treatment of erythrokeratodermia variabilis begins with an evaluation in Dermatology. Follow-up visits track how you are responding to care.
Treatment options
Diagnostic tests
Related articles
When to seek care
Questions about erythrokeratodermia variabilis? Call your nearest Weyland-Yutani location and ask for Dermatology.
Reference links
Eyelid disease
eyelid disease: An adnexa disease that is located_in the eyelid.
Classification
Ontology identifier: DOID:530 (Human Disease Ontology).
Classification path: disease of anatomical entity › integumentary system disease › skin disease.
Specialty: Dermatology
Broader conditions
More specific conditions
Medical codes
- ICD-10-CM: H02.9
- ICD-9-CM: 374.9
- MeSH: D005141
- SNOMED CT: 60113004
Care at Weyland-Yutani Health System
At Weyland-Yutani Health System, eyelid disease is managed by Dermatology with support from imaging, laboratory and rehabilitation services where needed.
Treatment options
Diagnostic tests
When to seek care
Seek a medical evaluation if you are concerned about eyelid disease. Bring a list of current medications and any previous test results.
Reference links