Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hypohidrotic X-linked ectodermal dysplasia |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Ectrodactyly-ectodermal dysplasia-clefting syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Hypohidrosis-diabetes insipidus syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Ectodermal dysplasia with hair-nail defect |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Ectodermal dysplasia-ocular malformation syndrome |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
Sandman-Andra syndrome |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Tricho-oculodermovertebral syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Oculodentodigital syndrome (disorder) |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Schoepf-Schulz-Passage syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Tricho-onychodental dysplasia |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Oculodento-osseous dysplasia - severe type |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Neurofibromatosis type 2 |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Mohr syndrome |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
4 |
Orofacial-digital syndrome IV |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
4 |
Oral-facial-digital syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Orofacial-digital syndrome III |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
4 |
Oculodento-osseous dysplasia - mild type |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Chondroectodermal dysplasia (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Robinson nail dystrophy-deafness syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Anonychia with bizarre flexural pigmentation |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Congenital junctional epidermolysis bullosa-pyloric atresia syndrome |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
3 |
Johanson-Blizzard syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Marshall syndrome |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
Kohlschutter's syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Congenital cutaneous angiomatosis |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
Schinzel-Giedion syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Congenital hamartoma of skin (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Moynahan's syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Keratoderma areata |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Palmoplantar hyperkeratosis sclerodactyly syndrome (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Keratoderma with mental retardation and spastic paraplegia |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Mutilating keratoderma |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Autosomal dominant mutilating keratoderma |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Congenital palmoplantar and perioral keratoderma of Olmsted |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Congenital keratoderma |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Hypodontia and nail dysgenesis |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Keratoderma with pachyonychia congenita |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Keratoderma punctata |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Normal moistness of skin |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Severe dry skin |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Oculodentodigital syndrome (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Congenital accessory skin tag |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
3 |
Oculodento-osseous dysplasia - severe type |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
7 |
Hay-Wells syndrome of ectodermal dysplasia |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
5 |
Oral-facial-digital syndrome |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
5 |
Oculodento-osseous dysplasia - mild type |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
7 |
Albinoidism |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Brown oculocutaneous albinism |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Rufous albinism |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Minimal pigment oculocutaneous albinism |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Yellow mutant oculocutaneous albinism |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Hermansky-Pudlak syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Tyrosinase-positive oculocutaneous albinism |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Autosomal dominant oculocutaneous albinism |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Congenital deficiency of pigment of skin |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Tyrosinase-negative oculocutaneous albinism |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Temperature-sensitive oculocutaneous albinism |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Cross syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
6 |
Oculocutaneous albinism |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Punctate oculocutaneous albinoidism |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Oculocutaneous albinoidism |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Encephalocraniocutaneous lipomatosis |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
2 |
Black locks, oculocutaneous albinism, AND deafness of the sensorineural type |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
2 |
Congenital fascial dystrophy |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Porokeratosis of Mibelli, linear unilateral type |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
5 |
Giant porokeratosis |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
4 |
Giant porokeratosis |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
5 |
Ehlers-Danlos syndrome, dominant type 4 |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Ehlers-Danlos syndrome, recessive type 4 |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Ehlers-Danlos syndrome, type 1 |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Ehlers-Danlos syndrome, procollagen proteinase resistant |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Porokeratosis of Mibelli, superficial disseminated type |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
5 |
Familial articular hypermobility syndrome (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Porokeratosis of Mibelli, plaque type |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
5 |
Ehlers-Danlos syndrome, type 2 |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Vascular Ehlers-Danlos syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Periodontal Ehlers-Danlos syndrome (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Ehlers-Danlos syndrome, dysfibronectinaemic |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Disseminated superficial actinic porokeratosis |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
5 |
Ehlers-Danlos syndrome, hydroxylysine-deficient |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Arthrochalasia Ehlers-Danlos syndrome (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Porokeratosis of Mibelli |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
4 |
Porokeratosis of Mibelli |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
5 |
X-linked Ehlers-Danlos syndrome |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Porokeratosis of Mantoux |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Cutis laxa, x-linked |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Ehlers-Danlos syndrome, non hydroxylysine deficient ocular type |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Ulerythema ophryogenes (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
5 |
Dyskeratosis congenita |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Symmetrical dyschromatosis of extremities |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Epidermolysis simplex superficialis |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Extensive congenital erosions, vesicles and reticulate scarring |
Finding site |
True |
Skin structure |
Inferred relationship |
Some |
1 |
Epidermolysis bullosa simplex with mottled pigmentation (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Progressive junctional epidermolysis bullosa (neurotrophic) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Congenital clubbing |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Porokeratosis of Mibelli, linear unilateral type |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |
Keratoderma due to Dowling-Meara type epidermolysis bullosa simplex (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Palmar pitting due to Darier disease |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Epidermolysis bullosa simplex, Ogna type (disorder) |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
3 |
Familial benign pemphigus |
Finding site |
False |
Skin structure |
Inferred relationship |
Some |
4 |