| Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
| Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome (disorder) |
interprète (attribut) |
False |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| Leucokeratosis of skin |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Leukokeratosis (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| Diffuse palmoplantar keratoderma with painful fissures |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Skin fragility, wooly hair, palmoplantar keratoderma syndrome (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| Focal palmoplantar keratoderma with joint keratoses (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Ichthyosis hystrix |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Severe ichthyoses |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Ichthyosis, oral and digital anomalies syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| Atypical ichthyosis vulgaris with hypogonadism |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Congenital ichthyosis with hypotrichosis syndrome (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Autosomal recessive ichthyosis (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Acral self-healing collodion baby (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Keratitis ichthyosis and deafness syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Syndromic recessive X-linked ichthyosis (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Autosomal recessive exfoliative ichthyosis (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Ichthyosis linearis circumflexa (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Ichthyosis hystrix gravior of Rheydt |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Congenital non bullous ichthyosiform erythroderma |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| Cutaneous syndrome with ichthyosis |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Bathing suit ichthyosis (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Limb reduction-ichthyosis syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Hystrix ichthyosis with deafness |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Ichthyosis, cerebellar degeneration and hepatosplenomegaly (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Ichthyosis bullosa of Siemens |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Non-bullous ichthyosiform erythroderma |
interprète (attribut) |
False |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Sjögren-Larsson syndrome (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Erythrodermic lamellar ichthyosis |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Ichthyosis cheek eyebrow syndrome (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Congenital cataract ichthyosis syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Ichthyosis vulgaris |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| ichtyose congénitale |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Sclerosing dysplasia of bone, ichthyosis, premature ovarian failure syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| Autosomal dominant ichthyosis (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Annular epidermolytic ichthyosis (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Lamellar ichthyosis (limited type) (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Senter syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Ichthyosis hystrix of Curth-Macklin |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Ichthyosis |
interprète (attribut) |
False |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Porcupine man |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Lamellar ichthyosis AND trichorrhexis invaginata syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Keratinopathic ichthyosis (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Autosomal dominant ichthyosis vulgaris |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| X-linked ichthyosis with steryl-sulfatase deficiency |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Localised bullous ichthyosiform erythroderma |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Ichthyosis prematurity syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Autosomal dominant lamellar ichthyosis |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Ichthyosis follicularis with alopecia and photophobia (IFAP) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Self-healing collodion baby (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| ichtyose lamellaire |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| Ichthyosis congenita with biliary atresia |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Non-erythrodermic lamellar ichthyosis |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| Ichthyosis, short stature, brachydactyly, microspherophakia syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
5 |
| Palmoplantar keratoderma, spastic paralysis syndrome (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Harlequin ichthyosis |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| Netherton's syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Hypotrichosis and deafness syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| maleformatio ectodermalis generalisata de Bafverstedt |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Bullous ichthyosiform erythroderma |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Rud's syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Hyperkeratotic eczema of palms and soles |
interprète (attribut) |
False |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
5 |
| Hyperkeratotic eczema of soles |
interprète (attribut) |
False |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Neu-Laxova syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| Rough skin (finding) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Rough skin of hands |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) |
interprète (attribut) |
False |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Keratoderma hereditarium mutilans with ichthyosis syndrome (disorder) |
interprète (attribut) |
False |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| Hypotrichosis with keratosis pilaris and lentiginosis |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Xeroderma of left eyelid |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| Xeroderma of right eyelid (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| Xeroderma of right upper eyelid |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Xeroderma of left upper eyelid |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| Harlequin fetus |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| Autosomal recessive epidermolytic ichthyosis (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Cutis gyrata syndrome of Beare and Stevenson |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Systematised linear porokeratosis |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
2 |
| Pityriasis rubra pilaris due to human immunodeficiency virus infection (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
6 |
| Erythrokeratodermia cardiomyopathy syndrome |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
4 |
| Congenital ichthyosis, microcephalus, tetraplegia syndrome (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome (disorder) |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
3 |
| O/E - rough skin |
interprète (attribut) |
False |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| Abnormal keratinization of hair follicle |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| Abnormal keratinisation of nail matrix |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| O/E - rough skin |
interprète (attribut) |
False |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| Abnormal keratinisation |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| Normal keratinization |
interprète (attribut) |
False |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| Decreased keratinization |
interprète (attribut) |
False |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| Increased keratinization |
interprète (attribut) |
False |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| Decreased keratinization |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| Normal keratinization |
interprète (attribut) |
True |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
| Abnormal keratinisation of nail matrix |
interprète (attribut) |
False |
Keratinization, function (observable entity) |
Inferred relationship |
Some |
1 |
FHIR