Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Thermal burn alopecia |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Alopecia |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Postpartum alopecia |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Cicatricial alopecia due to lichen planus of scalp (disorder) |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Alopecia due to disturbance of hair cycle (disorder) |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Massage alopecia (disorder) |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Cicatricial alopecia caused by ionising radiation |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
électrolyse de follicule pileux |
Procedure site - Direct (attribute) |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Congenital generalised alopecia |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Epilation NEC |
Procedure site - Direct (attribute) |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Congenital alopecia |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Taenzer's hair |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
poil atrophique |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Congenital alopecia with keratin cysts (disorder) |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Congenital ringed hair |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Diffuse alopecia |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Chronic telogen effluvium (disorder) |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Drug-induced hair color change (disorder) |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Congenital alopecia NOS |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Ulerythema ophryogenes (disorder) |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Drug-induced hair abnormality (disorder) |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Short anagen syndrome (disorder) |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Alopecia senilis |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Idiopathic hair dystrophy |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Syphilitic alopecia |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Uncombable hair syndrome |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Alopecia localis |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Sutural alopecia (disorder) |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Sheepshearer's hair sinus |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Hair sinus of breast |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Trichogram (procedure) |
Procedure site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Friction alopecia |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
transplantation capillaire |
Procedure site - Direct (attribute) |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Trichosporon beigelii infection (piedra) |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
|
Piedra |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
|
Fungal infection of hair |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
|
Cutting of hair |
Procedure site - Direct (attribute) |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Hypertrichosis of lower eyelid |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
|
Hypertrichosis of upper eyelid (disorder) |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
|
Persistent lanugo |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
Pili torti |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
Marie Unna syndrome |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Congenital ringed hair |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Congenital hypertrichosis lanuginosa (disorder) |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Hypertrichosis with congenital macrogingivae (disorder) |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Hypotrichosis with keratosis pilaris and lentiginosis |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Bayonet hair |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Pili annulati |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
BIDS brittle hair-impaired intellect-decreased fertility-short stature syndrome |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Congenital hypotrichia |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Genetic abnormality of hair shaft |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Taenzer's hair |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Beaded hair |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Congenital anomaly of hair |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Genetic defect of hair shaft (disorder) |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Congenital morphological disturbances of hair |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Uncombable hair syndrome |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Pili torti-deafness syndrome |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
Congenital hypertrichosis |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Total congenital alopecia |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
Vertical alopecia (disorder) |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Triangular alopecia (disorder) |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Congenital alopecia |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Congenital localised alopecia |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Congenital generalised alopecia |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Sutural alopecia (disorder) |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Atrichia congenita (disorder) |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Congenital alopecia with keratin cysts (disorder) |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Central centrifugal cicatricial alopecia (disorder) |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Curly hair, ankyloblepharon, nail dysplasia syndrome (disorder) |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
5 |
Ectodermal dysplasia with hair-nail defect |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
5 |
Tricho-oculodermovertebral syndrome |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
5 |
Congenital hypotrichia |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
Hypotrichosis with keratosis pilaris and lentiginosis |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
Chronic telogen effluvium (disorder) |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
An extremely rare genetic syndromic intellectual disability described in less than 20 families to date and characterized by total or partial alopecia associated with intellectual deficit. The syndrome can be associated with other anomalies such as seizures, sensorineural hearing loss, delayed psychomotor development, and/or hypertonia. |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
Pili torti-developmental delay-neurological abnormalities syndrome is characterized by growth and developmental delay, mild to moderate neurologic abnormalities, and pili torti. It has been described in a brother and his sister born to consanguineous Puerto Rican parents. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Pili torti-developmental delay-neurological abnormalities syndrome is characterized by growth and developmental delay, mild to moderate neurologic abnormalities, and pili torti. It has been described in a brother and his sister born to consanguineous Puerto Rican parents. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
Frontal fibrosing alopecia (FFA) is a rare variant of lichen planopilaris characterized by symmetrical, progressive, band-like anterior hair loss of the scalp. |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
Oculocerebral hypopigmentation syndrome, Preus type is a rare congenital syndrome characterized by skin and hair hypopigmentation, growth retardation, and intellectual deficit that are associated with a combination of various additional clinical anomalies such as ocular albinism, cataract, delayed neuro-psychomotor development, sensorineural hearing loss, dolicocephaly, high arched palate, widely spaced teeth, anemia, and/or nystagmus. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
Hypotrichosis simplex of the scalp (HSS) is characterized by diffuse progressive hair loss that is confined to the scalp. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
|
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 |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
|
Follicular hamartoma with alopecia and cystic fibrosis syndrome (disorder) |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
The patients are born with hair that falls out and is not replaced. Histologic studies show malformation of the hair follicles. Papillary lesions over most of the body and almost complete absence of hair are features. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
Sparse hair with short stature and skin anomaly syndrome |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
4 |
Autosomal recessive palmoplantar hyperkeratosis and congenital alopecia (PPK-CA) is a rare genetic skin disorder characterized by congenital alopecia and palmoplantar hyperkeratosis. It is usually associated with cataracts, progressive sclerodactyly and pseudo-ainhum. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
9 |
A rare endocrine disorder characterized by primary hypogonadism and partial alopecia. Females present with Mullerian hypoplasia, absent or streak ovaries, hypoplastic internal genitalia, primary amenorrhea, and sparse or absent axillary and pubic hair. Some patients also presented sparse eyebrows, microcephaly, flat occiput, dorsal kyphosis or mild intellectual disability. The only described male presents with germinal cell aplasia. Affected individual all present partial scalp alopecia. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
2 |
Hair that can be removed without resistance. |
Finding site |
True |
Hair structure (body structure) |
Inferred relationship |
Some |
1 |
A rare genetic skin disorder characterized by absence of scalp and body hair and palmoplantar keratoderma, without other hand complications. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
9 |
A rare genetic syndrome characterized by the association of congenital hypertrichosis in the anterior cervical region with peripheral sensory and motor neuropathy. Associated features may include retinal anomalies, spina bifida, kyphoscoliosis and hallux valgus, and developmental delay (one case). There have been no further descriptions in the literature since 1993. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
A rare multiple congenital anomalies syndrome characterized by association of congenital total alopecia, mild intellectual deficit and hypergonadotropic hypogonadism. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
A rare, syndromic, inherited retinal disorder characterized by cone-rod type congenital amaurosis, severe retinal dystrophy leading to visual impairment and profound photophobia (without night blindness), and trichomegaly (bushy eyebrows with synophrys, excessive facial and body hair including marked circumareolar hypertrichosis). There have been no further descriptions in the literature since 1989. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
A rare genetic syndromic intellectual disability that is characterized by congenital permanent alopecia universalis, intellectual disability, psychomotor epilepsy and periodontitis (pyorrhea). Total permanent alopecia and pyorrhea are invariably concomitant while intellectual disability and psychomotor epilepsy are observed in most patients. No other abnormality of nails or skin (apart from absence of hair) has been reported. Transmission is autosomal dominant. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
4 |
A rare ectodermal dysplasia syndrome, characterized by the association of choroidal atrophy (sometimes regional), together with other ectodermal dysplasia features including fine and sparse hair, absent or decreased lashes and eyebrows, and possibly mild visual loss and dysplastic/thick/grooved nails. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
8 |
Syndrome with the association of stubby, coarse, sparse and fragile hair, eyebrows and eyelashes with photosensitivity and nonprogressive intellectual deficit, without a demonstrable metabolic aberration. It has been described in three sisters born to consanguineous parents. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
Hidrotic ectodermal dysplasia, Halal type is a form of ectodermal dysplasia syndrome characterized by trichodysplasia, with absent eyebrows and eyelashes, onychodysplasia, mild retrognathia, abnormal dermatoglyphics (excess of whorls on fingertips, radial loop on finger, hypothenar pattern), intellectual disability and normal teeth and sweating. Additional variable manifestations include high implanted or prominent ears, mild hearing loss, supernumerary nipple, café-au-lait spots, keratosis pilaris, and irregular menses. To date, four individuals from 2 generations of a consanguineous family of Portuguese descent have been described in the literature. Males and females were equally affected. Hidrotic ectodermal dysplasia, Halal type is inherited in an autosomal recessive manner. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
4 |
This syndrome is characterized by the association of hypogonadotropic hypogonadism and frontoparietal alopecia. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
Rombo syndrome is characterized by vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, peripheral vasodilation with cyanosis and basal cell carcinomas. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
|
syndrome d'hypertrichose-faciès acromégaloïde |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
3 |
A rare, genetic, primary immunodeficiency due to a defect in adaptive immunity characterized by the triad of congenital athymia (resulting in severe T-cell immunodeficiency), congenital alopecia totalis and nail dystrophy. Patients present neonatal or infantile-onset, severe, recurrent, life-threatening infections and low or absent circulating T cells. Additional features reported include erythroderma, lymphoadenopathy, diarrhea and failure to thrive. |
Finding site |
False |
Hair structure (body structure) |
Inferred relationship |
Some |
5 |