Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hypohidrosis, enamel hypoplasia, palmoplantar keratoderma, intellectual disability syndrome |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
1 |
Corneal intraepithelial dyskeratosis, palmoplantar hyperkeratosis, laryngeal dyskeratosis syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
1 |
Leukokeratosis of skin |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Leukokeratosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
1 |
Diffuse palmoplantar keratoderma with painful fissures |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Skin fragillity, woolly hair, palmoplantar keratoderma syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
4 |
Focal palmoplantar keratoderma with joint keratoses |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Ichthyosis hystrix |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Severe ichthyoses |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Ichthyosis, oral and digital anomalies syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
4 |
Atypical ichthyosis vulgaris with hypogonadism |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Congenital ichthyosis with hypotrichosis syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Autosomal recessive ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Acral self-healing collodion baby |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Keratitis ichthyosis and deafness syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Syndromic recessive X-linked ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Autosomal recessive exfoliative ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Ichthyosis linearis circumflexa |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Ichthyosis hystrix gravior of Rheydt |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
2 |
Congenital non bullous ichthyosiform erythroderma |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Neonatal sclerosing cholangitis, ichthyosis, hypotrichosis syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
4 |
Cutaneous syndrome with ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Bathing suit ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Limb reduction-ichthyosis syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Autosomal recessive keratitis-ichthyosis-deafness syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Hystrix ichthyosis with deafness |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
2 |
Ichthyosis, cerebellar degeneration and hepatosplenomegaly |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Ichthyosis bullosa of Siemens |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Non-bullous ichthyosiform erythroderma |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
2 |
Sjögren-Larsson syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Erythrodermic lamellar ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Ichthyosis cheek eyebrow syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Congenital cataract ichthyosis syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Ichthyosis vulgaris |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Ichthyosis, alopecia, eclabion, ectropion, intellectual disability syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
4 |
X-linked intellectual disability, hypogonadism, ichthyosis, obesity, short stature syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Congenital ichthyosis of skin |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Osteosclerosis, ichthyosis, premature ovarian failure syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
4 |
Autosomal dominant ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Annular epidermolytic ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Lamellar ichthyosis (limited type) |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Senter syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Ichthyosis hystrix of Curth-Macklin |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Ichthyosis |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
2 |
Porcupine man |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
2 |
Lamellar ichthyosis AND trichorrhexis invaginata syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Keratinopathic ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Autosomal dominant ichthyosis vulgaris |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
X-linked ichthyosis with steryl-sulfatase deficiency |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Localised bullous ichthyosiform erythroderma |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Ichthyosis prematurity syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Autosomal dominant lamellar ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Ichthyosis follicularis with alopecia and photophobia (IFAP) |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Self-healing collodion baby |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Lamellar ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Ichthyosis, intellectual disability, dwarfism, renal impairment syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
4 |
Ichthyosis congenita with biliary atresia |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Non-erythrodermic lamellar ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
4 |
Ichthyosis, short stature, brachydactyly, microspherophakia syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
5 |
Palmoplantar keratoderma, spastic paralysis syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Harlequin ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
4 |
Netherton's syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Hypotrichosis and deafness syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Maleformatio ectodermalis generalisata of Bafverstedt |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Bullous ichthyosiform erythroderma |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Rud's syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Hyperkeratotic eczema of hands and feet |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
5 |
Hyperkeratotic eczema of soles |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
3 |
Neu-Laxova syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
4 |
Rough skin |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Rough skin of hands |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Keratoderma hereditarium mutilans with ichthyosis syndrome |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
3 |
Keratoderma hereditarium mutilans with ichthyosis syndrome |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
4 |
Hypotrichosis with keratosis pilaris and lentiginosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Xeroderma of left eyelid |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
4 |
Xeroderma of right eyelid |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
4 |
Xeroderma of right upper eyelid |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
3 |
Xeroderma of left upper eyelid |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
3 |
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
1 |
Harlequin fetus |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
4 |
Autosomal recessive epidermolytic ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Cutis gyrata syndrome of Beare and Stevenson |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Systematised linear porokeratosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Pityriasis rubra pilaris due to human immunodeficiency virus infection |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Lichenoid keratosis |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
686841737 |
Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
6 |
Erythrokeratodermia cardiomyopathy syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
4 |
Congenital ichthyosis, microcephalus, tetraplegia syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Congenital ichthyosis, intellectual disability, spastic quadriplegia syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
PLACK syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
5 |
Generalised inflammatory peeling skin syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
4 |
Generalised non-inflammatory peeling skin syndrome |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
3 |
Ichthyosis hystrix gravior |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Juvenile pityriasis rubra pilaris |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Acquired paraneoplastic ichthyosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Adult pityriasis rubra pilaris |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
Terra firma-forme dermatosis |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
2 |
O/E - rough skin |
Interprets |
False |
Keratinisation |
Inferred relationship |
Some |
1 |
Abnormal keratinisation of hair follicle |
Interprets |
True |
Keratinisation |
Inferred relationship |
Some |
1 |