Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Disturbance of hair cycle |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|
Malposition of lashes |
Is a |
False |
Disorder of hair growth |
Inferred relationship |
Some |
|
Congenital distichiasis |
Is a |
False |
Disorder of hair growth |
Inferred relationship |
Some |
|
Atrichia |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|
Hypertrichosis |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|
Hypotrichosis |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|
Alopecia |
Is a |
False |
Disorder of hair growth |
Inferred relationship |
Some |
|
Distichiasis |
Is a |
False |
Disorder of hair growth |
Inferred relationship |
Some |
|
Other hair and hair follicle diseases |
Is a |
False |
Disorder of hair growth |
Inferred relationship |
Some |
|
Hair and hair follicle disease NOS |
Is a |
False |
Disorder of hair growth |
Inferred relationship |
Some |
|
Hirsutism (disorder) |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|
Trichiasis (disorder) |
Is a |
False |
Disorder of hair growth |
Inferred relationship |
Some |
|
Congenital alopecia |
Is a |
False |
Disorder of hair growth |
Inferred relationship |
Some |
|
A rare ectodermal dysplasia syndrome characterized by congenital onychodystrophy (particularly of the distal nail) and severe hypotrichosis with alopecia involving the eyebrows, eyelashes and body hair. Scalp, beard, pubic and axillary hair is brittle and shows a twisting pattern on electron microscopy. There have been no further descriptions in the literature since 1991. |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|
An uncommon transitory hair shaft dysplasia characterized by segmental duplication of the hair shaft: a ramification generates two parallel branches which fuse to form a single shaft again. Each branch is covered by its own cuticle. |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome, also known as Oliver-McFarlane syndrome, is an extremely rare genetic disorder characterized by hair abnormalities, severe chorioretinal atrophy, hypopituitarism, short stature, and intellectual disability. |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|
Odonto-onychial dysplasia with alopecia |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|
A rare syndromic intellectual deficiency characterized by psychomotor delay, severe progressive spastic quadriplegia, microcephaly, and a Hallermann-Streiff-like phenotype including absence of eyebrows and eyelashes, glaucoma, and small, beaked nose. Structural central nervous system abnormalities (cervical spinal cyst, occipital cranium bifidum occulatum) were additional findings. There have been no further descriptions in the literature since 1974. |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|
Congenital absence of eyelash |
Is a |
False |
Disorder of hair growth |
Inferred relationship |
Some |
|
Ulerythema ophryogenes (disorder) |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|
Agenesis of cilia of eyelid (disorder) |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|
Hypotrichosis with keratosis pilaris and lentiginosis |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|
Congenital hypoplasia of eyebrow |
Is a |
True |
Disorder of hair growth |
Inferred relationship |
Some |
|