Public registry
Nodes
Browse canonical concepts by label, domain, node type, prefix and encoded class.
Current membership scope: Secondary membership only
| Concept | Node type | Base domain | Matched membership | Identifier |
|---|---|---|---|---|
| Facial Dermatoses Skin diseases involving the FACE. | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170069 |
| Focal Facial Dermal Dysplasias A heterogenous group of genetic disorders characterized by scar-like atrophic lesions on the temple region of the head including preauricular area. L… | Pathologic Condition | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160013 |
| Folliculitis Inflammation of follicles, primarily hair follicles. | Inflammatory Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170074 |
| Foot Dermatoses Skin diseases of the foot, general or unspecified. | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170070 |
| Foot Ulcer Lesion on the surface of the skin of the foot, usually accompanied by inflammation. The lesion may become infected or necrotic and is frequently asso… | Pathologic Condition | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170071 |
| Fox-Fordyce Disease Chronic pruritic disease, usually in women, characterized by small follicular papular eruptions in APOCRINE GLANDS areas. It is caused by obstruction… | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170153 |
| Granuloma Annulare Benign granulomatous disease of unknown etiology characterized by a ring of localized or disseminated papules or nodules on the skin and palisading h… | Pathologic Condition | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170008 |
| Guttate Psoriasis A skin condition, typically emerges suddenly and frequently occurs after an infection such as STREPTOCOCCAL INFECTION. While prevalent among children… | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170133 |
| Hair Diseases Diseases affecting the orderly growth and persistence of hair. | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170073 |
| Hand Dermatoses Skin diseases involving the HANDS. | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170081 |
| Hand-Foot Syndrome Chemotherapy-induced dermal side effects that are associated with the use of various CYTOSTATIC AGENTS. Symptoms range from mild ERYTHEMA and/or PARE… | Syndrome | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170056 |
| Hidradenitis The inflammation of a sweat gland (usually of the apocrine type). The condition can be idiopathic or occur as a result of or in association with anot… | Inflammatory Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170149 |
| Hirsutism A condition observed in WOMEN and CHILDREN when there is excess coarse body hair of an adult male distribution pattern, such as facial and chest area… | Pathologic Condition | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170075 |
| Hydroa Vacciniforme A vesicular and bullous eruption having a tendency to recur in summer during childhood and commonly appearing on sun-exposed skin. The lesions are su… | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170099 |
| Hyperhidrosis Excessive sweating. In the localized type, the most frequent sites are the palms, soles, axillae, inguinal folds, and the perineal area. Its chief ca… | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170150 |
| Hyperkeratosis, Epidermolytic A form of congenital ichthyosis inherited as an autosomal dominant trait and characterized by ERYTHRODERMA and severe hyperkeratosis. It is manifeste… | Congenital Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160044 |
| Hyperpigmentation Excessive pigmentation of the skin, usually as a result of increased epidermal or dermal melanin pigmentation, hypermelanosis. Hyperpigmentation can … | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170105 |
| Hypertrichosis Excessive hair growth at inappropriate locations, such as on the extremities, the head, and the back. It is caused by genetic or acquired factors, an… | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170076 |
| Hypohidrosis Abnormally diminished or absent perspiration. Both generalized and segmented (reduced or absent sweating in circumscribed locations) forms of the dis… | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170151 |
| Hypopigmentation A condition caused by a deficiency or a loss of melanin pigmentation in the epidermis, also known as hypomelanosis. Hypopigmentation can be localized… | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170109 |
| Hypotrichosis Presence of less than the normal amount of hair. (Dorland, 27th ed) | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170077 |
| Ichthyosis Any of several generalized skin disorders characterized by dryness, roughness, and scaliness, due to hypertrophy of the stratum corneum epidermis. Mo… | Congenital Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160042 |
| Ichthyosis Bullosa of Siemens An autosomal dominant form of ichthyosis characterized by generalized reddening of the skin (ERYTHEMA) and widespread blistering. The disease shows s… | Congenital Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160046 |
| Ichthyosis Vulgaris Most common form of ICHTHYOSIS characterized by prominent scaling especially on the exterior surfaces of the extremities. It is inherited as an autos… | Congenital Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160047 |
| Ichthyosis, Lamellar A chronic, congenital ichthyosis inherited as an autosomal recessive trait. Infants are usually born encased in a collodion membrane which sheds with… | Congenital Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160045 |
| Ichthyosis, X-Linked Chronic form of ichthyosis that is inherited as a sex-linked recessive trait carried on the X-chromosome and transmitted to the male offspring. It is… | Congenital Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160048 |
| Immersion Foot A condition of the feet produced by prolonged exposure of the feet to water. Exposure for 48 hours or more to warm water causes tropical immersion fo… | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170072 |
| Incontinentia Pigmenti A genodermatosis occurring mostly in females and characterized by skin changes in three phases - vesiculobullous, verrucous papillomatous, and macula… | Congenital Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:160015 |
| Intertrigo A superficial dermatitis occurring on skin surfaces in contact with each other, such as the axillae, neck creases, intergluteal fold, between the toe… | Disorder | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170061 |
| Keloid A sharply elevated, irregularly shaped, progressively enlarging scar resulting from formation of excessive amounts of collagen in the dermis during c… | Pathologic Condition | Pathology | Integumentary System [curated_secondary] | AMW:DIS:170005 |