Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Xanthosis (morphologic abnormality) |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Fibrosiderotic nodule |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Heavy metal pigmentation |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ferrocalcinotic deposition |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Haematin pigmentation |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hematoidin pigmentation |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Melanosis |
Is a |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hyperpigmentation (morphologic abnormality) |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Melanin pigmentation |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Lipochrome pigmentation (morphologic abnormality) |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hemosiderin pigmentation |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hemofuscin pigmentation |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Bile pigmentation (morphologic abnormality) |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Kernicterus (morphologic abnormality) |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mineralized neurons (morphologic abnormality) |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Pseudomelanosis (morphologic abnormality) |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Lipogenic pigmentation |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ceroid pigmentation |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hemoglobin pigmentation |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Porphyrin pigmentation |
Is a |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypopigmentation disorder |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Villonodular synovitis of multiple sites |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, group B |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
pigmentation paludéenne |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Malarial pigment deposition (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Amelogenesis imperfecta, pigmented hypomaturation type (disorder) |
Associated morphology |
True |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Drug-induced pigmentation |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Drug pigmentation |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Schistosomal pigment deposition |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Occupational tattoo |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Collier's stripes |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Occupational vitiligo |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pseudoatrophoderma colli |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Drug-induced hypomelanosis |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Symmetrical progressive leucopathy |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acantholytic dyskeratotic epidermal nevus |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Nevus striatus symmetricus of thumbs |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Epidermal nevus syndrome |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Miscellaneous disorders of skin pigmentation |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Mucosal lentiginosis |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pigmentation of fingers (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare type of keratinopathic ichthyosis characterised by the presence of severe hyperkeratotic lesions and palmoplantar keratoderma. The skin is usually normal at birth. The disease starts in early childhood with severe hyperkeratosis of yellow-brown or grey colour, and of spiky, cobblestone-like (hystrix) or verrucous appearance. Contrary to other keratinopathic ichthyoses, no skin fragility/blister formation or erythroderma is present. The disease results from heterozygous frameshift mutation in a section of the KRT1 gene encoding keratin 1 (K1). These mutations lead to an abnormal supramolecular organisation of keratin intermediate filaments and may be related to defects in cytoplasmic trafficking and integrity of cellular structures such as organelles and nucleus. Transmission is autosomal dominant but some sporadic cases have been reported. |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Ichthyosis hystrix Bäfverstedt type (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Ichthyosis hystrix gravior of Rheydt |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Hystrix ichthyosis with deafness |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Porcupine man |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
De Sanctis-Cacchione syndrome |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acquired disorder of skin colour |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Post-inflammatory hypopigmentation |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chemically-induced hypomelanosis (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Diffuse tenosynovial giant cell tumor of lower limb |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Café au lait spots |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pigmented xerodermoid |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Idiopathic guttate hypomelanosis |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Anterior corneal pigmentation |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Chlorpromazine pigmentation |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Skin hypopigmented |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Achromia of skin |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
ictère périnatal causé par une hémolyse excessive |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Xeroderma pigmentosum, group C (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, group G |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Progressive pigmentary dermatosis |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Leukoderma |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Xeroderma pigmentosum, group F |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Tattoo granuloma |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Xeroderma pigmentosum, group A |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Dubin-Johnson syndrome |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Xeroderma pigmentosum (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Poikiloderma of Civatte |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Disorder of skin pigmentation |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Linear sebaceous nevus sequence |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Conjunctival argyrosis |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Stromal corneal pigmentation |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Syphilitic leukoderma |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, group E (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Vitiligo of pinta (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
3 |
Vitiligo |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
ictère périnatal dû à une anémie hémolytique héréditaire |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hemolytic jaundice |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Progressive pigmentary dermatosis of Schamberg |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Conjunctival pigmentation (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Ichthyosis hystrix (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, group D |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Neonatal jaundice due to delayed conjugation from delayed development of conjugating system (finding) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ephelides |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Nevus unius lateris |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
5 |
Disorder of central nervous system due to xeroderma pigmentosum (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Neonatal jaundice associated with preterm delivery (finding) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Perinataler Ikterus verursacht durch Gallenpfropf-Syndrom |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Tattoo |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Non-neurologic xeroderma pigmentosum |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Erythromelanosis follicularis of face AND/OR neck (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Vitiligo of eyelid (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Xeroderma pigmentosum, variant form |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Argyria of skin |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Neurofibromatosis type 1 (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Postinflammatory skin pigmentation change |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
2 |
Application site pigmentation changes |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
synovite villonodulaire pigmentée |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |
Acquired anterior capsular pigmentation (disorder) |
Associated morphology |
False |
Structure showing abnormal deposition of pigment (morphologic abnormality) |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
1 |