386045008: Hair structure (body structure)

SNOMED CT Concept\Body structure (body structure)\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\An anatomical structure that consists of the maximal set of organ parts so connected to one another that together they constitute a self-contained unit of macroscopic anatomy, distinct both morphologically and functionally from other such units. Together with other organs, an organ constitutes an organ system or a body part. An organ is divisible into organ parts but not organs (examples: femur, biceps, liver, heart, aorta, sciatic nerve, ovary).\Skin structure\Skin appendage structure (body structure)\Hair structure (body structure)

\Body system structure\Structure of subdivision of organ system (body structure)\Skin and/or subcutaneous tissue structure (body structure)\Skin structure\Skin appendage structure (body structure)\Hair structure (body structure)
\Body system structure\Structure of skin and/or mucous membrane (body structure)\Region consisting of all body skin and directly related mucosa but excluding mucosa within the body such as the mucous membrane of the urinary bladder.\Skin structure\Skin appendage structure (body structure)\Hair structure (body structure)
\Body system structure\Structure of skin and/or surface epithelium (body structure)\Skin structure\Skin appendage structure (body structure)\Hair structure (body structure)
\Body system structure\Structure of integumentary system (body structure)\Integumentary system part (body structure)\Skin and/or subcutaneous tissue structure (body structure)\Skin structure\Skin appendage structure (body structure)\Hair structure (body structure)

\Body tissue structure\Structure of soft tissue (body structure)\Skin and/or subcutaneous tissue structure (body structure)\Skin structure\Skin appendage structure (body structure)\Hair structure (body structure)

\Body region structure\Skin and/or subcutaneous tissue structure (body structure)\Skin structure\Skin appendage structure (body structure)\Hair structure (body structure)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

1460224016 Hair structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

1480232019 Hair structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

1491447017 Hair en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Hair structure (body structure)	Is a	Structure of hair of skin region (body structure)	false	Inferred relationship	Some
Hair structure (body structure)	Is a	Hair appendage structure	false	Inferred relationship	Some
Hair structure (body structure)	partie de	Entire skin	false	Inferred relationship	Some
Hair structure (body structure)	Is a	Skin appendage structure (body structure)	true	Inferred relationship	Some
Hair structure (body structure)	partie de	Entire integumentary system	false	Additional relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Barber-Say syndrome (disorder)	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	2
Female hirsutism	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Non-androgenic hypertrichosis	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Hypertrichosis lanuginosa	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Hypertrichosis pinnae auris	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Non-androgenic hypertrichosis co-occurrent and due to genetic disease (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Disorder of hair growth	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Androgen-dependent hirsutism	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Familial hirsutism (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Hypertrichosis of eyelid	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Madarosis of eyebrow (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Hirsuties papillaris vulvae	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Madarosis of eyelid	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	1
Hypertrichosis in malnutrition (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Hypertrichosis in anorexia nervosa (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Hypertrichosis in hyperthyroidism (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Hypertrichosis in hypothyroidism (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Hypertrichosis in porphyria (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Constitutionally-determined racial hirsutism (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Telogen effluvium	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Androgen-independent hirsutism	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Extreme insulin resistance with acanthosis nigricans, hirsutism AND abnormal insulin receptors	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Cicatricial trichiasis	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	2
Hypotrichosis of eyelid	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	1
Disturbance of hair cycle	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Loose anagen hair syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
A rare autosomal dominant disorder characterized by a generalized enlargement of the gingiva occurring at birth or during childhood that is associated with generalized hypertrichosis developing at birth, during the first years of life, or at puberty and predominantly affecting the face, upper limbs, and midback.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	2
Telogen effluvium of the newborn (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Acute telogen effluvium (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	2
à l'examen : hirsutisme	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	1
Hypertrichosis of lower eyelid	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
A rare form of localized hypertrichosis characterized by hair growth near the laryngeal prominence during childhood.	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	2
Trichiasis (disorder)	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	2
Telogen hair loss caused by drug	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Anagen effluvium caused by drug (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Hypotrichosis following infectious disease (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	2
Rombo syndrome is characterized by vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, peripheral vasodilation with cyanosis and basal cell carcinomas.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Bilateral trichiasis	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	1
Atrichia	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Hirsutism (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Hypertrichosis cubiti is a rare hair anomaly characterized by symmetrical, congenital or early-onset, bilateral hypertrichosis localized on the extensor surfaces of the upper extremities (especially the elbows). Short stature, or other abnormalities, such as developmental delay, facial anomalies and intellectual disability, may or may not be associated.	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	4
A rare cutaneous paraneoplastic disease characterised by the presence of excessive lanugo-type hair on the glabrous skin of face, neck, trunk and limbs that can be associated with additional clinical features such as burning glossitis, papillary hypertrophy of the tongue, diarrhoea, dysgeusia, and/or weight loss. It is associated with lymphoma or cancer of the gastrointestinal system, urinary tract, lung, breast, uterus or ovary.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
A rare primary immunodeficiency disorder characterized by the association of alopecia areata totalis and antibody deficiency (congenital agammaglobulinemia or incomplete antibody deficiency syndrome), manifesting with recurrent infections. There have been no further descriptions in the literature since 1976.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Lanugo hair	Is a	True	Hair structure (body structure)	Inferred relationship	Some
A rare primary bone dysplasia characterized by the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular, hyperpigmented dermopathy and a white forelock.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	3
Abnormal hair finding (finding)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	2
A syndromic genetic deafness characterized by erythrokeratoderma, hypotrichosis, nail dystrophy and sensorineural hearing loss. Erythema, recurrent skin infections and mucositis have also been associated.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	2
A rare, genetic, ectodermal dysplasia syndrome characterized by skin, hair and nail anomalies (i.e. generalized ichthyosis, congenital alopecia universalis, dystrophic, convex nails), associated with hypohidrosis without hyperthermia, intellectual disability, seizures, and skeletal (e.g. proportionate short stature, platyspondyly) and intestinal (e.g. congenital aganglionic megacolon) anomalies. Facial dysmorphism includes frontal bossing, blepharophimosis, large ears, low nasal bridge and small nose. There have been no further descriptions in the literature since 1992.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	2
Schinzel-Giedion syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Hypohidrotic X-linked ectodermal dysplasia	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Roselli-Gulienetti ectodermal dysplasia (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Basan syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Greither type of ectodermal dysplasia	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Anonychia with bizarre flexural pigmentation	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	5
Tricho-onychodental dysplasia	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
syndrome de Schoef-Schulz-Passage	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	4
Odonto-onychial dysplasia with alopecia	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	6
Fried's tooth and nail syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Hypodontia and nail dysgenesis	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	5
dysplasie dermodentaire	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	4
Salamon's syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Ectodermal dysplasia, syndactyly and pili torti	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Dwarfism, alopecia, pseudoanodontia, cutis laxa	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Hypohidrosis-diabetes insipidus syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	5
Odontotrichomelic syndrome (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1
Berlin syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	2
Flynn-Aird syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	2
Trichodental syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	2
Cranioectodermal dysplasia	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	3
Ulceration of lash follicles	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	2
Collarettes of lash follicles	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	2
Eyelash follicle finding	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	2
Ectodermal dysplasia with hair-tooth-nail-sweating defect	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	3
Ectodermal dysplasia with hair-tooth-nail defects (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	3
Ectodermal dysplasia with hair-tooth defects	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	3
Oculodentodigital syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	5
Tricho-dento-osseous syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Ectrodactyly-ectodermal dysplasia-clefting syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	5
Odonto-onycho-dermal dysplasia (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Ectodermal syndrome with hair-tooth-sweating defects (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	3
Ectodermal syndrome with hair-sweating defects (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	2
Chondroectodermal dysplasia	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	6
Hay-Wells syndrome of ectodermal dysplasia	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	5
Hidrotic ectodermal dysplasia syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Anhidrotic ectodermal dysplasia with immune deficiency (disorder)	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	7
Johanson-Blizzard syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	2
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	5
Tricho-retino-dento-digital syndrome is an autosomal dominant ectodermal dysplasia syndrome, characterized by uncombable hair syndrome, congenital hypotrichosis and dental abnormalities such as oligodontia or hyperdontia, and associated with early-onset cataract, retinal pigmentary dystrophy, and brachydactyly with brachymetacarpia. Furthermore, hyperactivity and a mild intellectual deficit have been reported in affected patients.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	2
This syndrome has characteristics of congenital absence of the teeth and sparse or absent hair. Taurodontia is also present in the majority of cases. The syndrome has been described in less than 15 patients from different families.	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	4
A rare ectodermal dysplasia syndrome characterized by severe arthrogryposis, multiple ectodermal dysplasia features, cleft lip/palate, facial dysmorphism, growth deficiency and a moderate delay of psychomotor development. Ectodermal dysplasia manifestations include sparse, brittle and hypopigmented hair, xerosis, multiple nevi, small conical shaped teeth and hypodontia, and facial dysmorphism with blepharophimosis, deep-set eyes and micrognathia.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	5
A rare ectodermal dysplasia syndrome characterized by a variably severe clinical picture comprising dry, thin skin, onychodysplasia, trichodysplasia, and dental abnormalities (such as hypodontia, microdontia, and persistence of deciduous teeth). There have been no further descriptions in the literature since 1990.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
A rare multiple congenital anomalies/dysmorphic syndrome characterized by intellectual disability, severe visual impairment due to ocular malformations (microphthalmos and microcornea with sclerocornea), short stature, hypotrichosis, dental anomalies, and dysmorphic facial features (such as a narrow nasal bridge with marked distal flaring and low-set, protruding ears). There have been no further descriptions in the literature since 1992.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
A rare, genetic, multiple congenital anomalies syndrome characterized by growth retardation, alopecia, pseudoanodontia and ocular manifestations.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
A rare multiple congenital anomalies/dysmorphic syndrome characterized by short stature and particularly pronounced shortening of the third to fifth metacarpals and metatarsals, congenital anodontia, sparse hair, dyspigmentation of the skin, hypoplastic nipples and underdeveloped external genitals in females, and multiple ocular abnormalities (such as distichiasis, strabismus, nystagmus, lenticular opacities, and severe myopia, among others). Dysmorphic craniofacial features include brachycephaly, downslanting palpebral fissures, broad nasal root, low-set ears, and small maxilla and prominent mandible. There have been no further descriptions in the literature since 1968.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	2
A rare ectodermal dysplasia syndrome characterized by bilateral retinitis pigmentosa, trichodysplasia (generalized hypotrichosis, structural changes), dental anomalies, onychodysplasia, and dry and scaly skin. There have been no further descriptions in the literature since 1988.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	5
A rare ectodermal dysplasia syndrome characterized by neonatal teeth, trichodystrophy (with straw-like, discolored and fragile hair), onychodystrophy, and malformation of the hands and feet consisting of simian-like hands with transverse palmar creases and prominent interdigital folds, brachydactyly, and marked shortness of the first metacarpal and metatarsal bones with hypoplasia of the distal phalanges. There have been no further descriptions in the literature since 1997.	Finding site	False	Hair structure (body structure)	Inferred relationship	Some	3
A rare autosomal dominant ectodermal dysplasia syndrome characterized by premolar aplasia, hyperhidrosis, and premature graying of the hair. Additional features may include a narrow palate, hypoplastic nails, eyebrow anomalies, a unilateral simian crease, and poorly formed dermatoglyphics.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Ectodermal dysplasia, trichoodontoonychial type is a form of ectodermal dysplasia with hair, teeth and nail involvement characterized predominantly by hypodontia, hypotrichosis, delayed hair growth and brittle nails. Additionally, focal dermal hypoplasia, irregular hyperpigmentation, hypoplastic or absent nipples, amastia, hearing impairment, congenital hip dislocation and asthma have been associated. There have been no further descriptions in the literature since 1996.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	4
Teebi-Shaltout syndrome is a rare, genetic, development defect during embryogenesis malformation syndrome characterized by association of characteristic facial features (including abnormal head shape with narrow forehead, hypertelorism, telecanthus, small earlobes, broad nasal bridge and tip, underdeveloped ala nasi, small/wide mouth and high/cleft palate), ectodermal dysplasia (including oligodontia with delayed dentition, slow growing hair and reduced sweating) and skeletal abnormalities including camptodactyly and caudal appendage. Short stature and abnormal palmar creases are additional clinical features.	Finding site	True	Hair structure (body structure)	Inferred relationship	Some	1

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

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Id	Description	Lang	Type	Status	Case?	Module
1460224016	Hair structure (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1480232019	Hair structure	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1491447017	Hair	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core