Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Normal variation in cutaneous pigmentation |
Is a |
False |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
Dyschromatosis universalis |
Is a |
True |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
Naegeli-Franceschetti-Jadassohn syndrome |
Is a |
True |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
Symmetrical dyschromatosis of extremities |
Is a |
True |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
Zosteriform reticulate hyperpigmentation |
Is a |
False |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
Dermatopathia pigmentosa reticularis |
Is a |
True |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
Acromelanosis |
Is a |
True |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
X-linked reticulate pigmentary disorder is an extremely rare skin disease described in only four families to date and characterized in males by diffuse reticulate brown hyperpigmented skin lesions developing in early childhood and a variety of systemic manifestations (recurrent pneumonia, corneal opacification, gastrointestinal inflammation, urethral stricture, failure to thrive, hypohidrosis, digital clubbing, and unruly hair and flared eyebrows), while in females, there is only cutaneous involvement with the development in early childhood of localized brown hyperpigmented skin lesions following the lines of Blaschko. This disease was first considered as a cutaneous amyloidosis, but amyloid deposits are an inconstant feature. |
Is a |
False |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
Terminal osseous dysplasia-pigmentary defects syndrome is characterized by malformation of the hands and feet, pigmentary skin lesions on the face and scalp and digital fibromatosis. |
Is a |
True |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
A rare genetic congenital limb malformation syndrome with characteristics of short stature, sparse scalp hair, hypoplastic, proximally placed thumbs and skin hyperpigmentation with areas of 'raindrop' depigmentation. Presence of a single, upper central incisor has also been reported. There have been no further descriptions in the literature since 1988. |
Is a |
True |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
A rare genetic malformation syndrome with characteristics of microcephaly, borderline intellectual disability, hyperpigmentation of the skin, short stature, and ventricular extrasystoles. Cardiac syncope may also be associated. There have been no further descriptions in the literature since 1975. |
Is a |
True |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
Syndrome with characteristics of the association of osteopathia striata (longitudinal striations through most of the long bones) with a macular hyperpigmented dermopathy and a white forelock. It has been observed in a woman and her two daughters, whereas her son is unaffected. X-linked or autosomal dominant inheritance is proposed. |
Is a |
True |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
Hereditary benign acanthosis nigricans |
Is a |
True |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
Hereditary benign acanthosis nigricans with insulin resistance |
Is a |
True |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|
A rare genetic disease characterized by the presence of multiple café-au-lait macules and elevated rates of sister chromatid exchange demonstrated on cytogenetic testing. Pre- and postnatal growth deficiency with short stature, microcephaly, mild developmental delay, cardiomyopathy, and symptomatic gastro-esophageal reflux have also been described, while malar rash is typically absent. |
Is a |
True |
Inherited cutaneous hyperpigmentation |
Inferred relationship |
Some |
|