Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Carney complex (disorder) |
Is a |
False |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Gastrocutaneous syndrome |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Facial dysmorphism, anorexia, cachexia, eye and skin anomalies syndrome (disorder) |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Inherited cutaneous hyperpigmentation |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Severe growth deficiency, strabismus, extensive dermal melanocytosis, intellectual disability syndrome |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Neurofibromatosis type 6 |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Hereditary distal onycholysis |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Congenital isolated onychodysplasia |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Birt Hogg Dubé syndrome |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Congenital insensitivity to pain, hyperhidrosis, absence of cutaneous sensory innervation (disorder) |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Exostosis, anetoderma, brachydactyly type E syndrome (disorder) |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Full schwannomatosis |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Autosomal recessive hyper-IgE syndrome due to ZNF341 deficiency |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Coagulation factor XII-associated cold autoinflammatory syndrome (disorder) |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Caspase recruitment domain family member 11-associated atopy with dominant interference of nuclear factor kappa-B signaling syndrome (disorder) |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|
Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA gain of function mutation |
Is a |
True |
Hereditary disorder of the integument |
Inferred relationship |
Some |
|