Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Congenital sixth nerve palsy (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cryptophthalmos (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Ankyloblepharon filiforme adnatum (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital tarsal kink (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Euryblepharon (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital miosis (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital mydriasis (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital iris ectropion (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
dysplasie du cortex cérébral |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Nicolaides-Baraitser syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Pena-Shokeir syndrome type I (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Smith-Magenis syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Epidermolysis bullosa acquisita, classical acral type (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Epidermolysis bullosa acquisita, bullous pemphigoid-like (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Epidermolysis bullosa acquisita, cicatricial pemphigoid-like (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Epidermolysis bullosa acquisita, Brunsting-Perry type (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Epidermolysis bullosa acquisita, oral mucosal involvement (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Gouty tophus (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Chronic tophaceous gout of digit |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Sporadic porphyria cutanea tarda (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Immunodeficiency with multicarboxylase deficiency |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
3 |
Congenital malignant melanoma (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital vascular malformation of skin |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Acquired cutaneous vascular malformation |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Developmental anomaly of vitelline duct (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Autosomal dominant ichthyosis (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
X-linked recessive ichthyosis |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Autosomal recessive ichthyosis (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Punctate palmoplantar keratoderma (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Genetic defect of hair shaft (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Inherited epidermolysis bullosa |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital/hereditary cutis laxa |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Genetic disorder of lipid storage (disorder) |
Occurrence |
True |
Congenital |
Inferred relationship |
Some |
1 |
Congenital vascular malformation due to inherited syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Developmental malformation of branchial arch (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Acquired arteriovenous malformation of the skin (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Fordyce spots of lips (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Fordyce spots of buccal mucosa (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Fordyce spots of penis (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Fordyce spots of vulva (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Post-inflammatory cutis laxa (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cutis laxa following urticaria-angioedema (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cutis laxa following hypersensitivity reaction (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cutis laxa with complement deficiency (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Solitary infantile myofibromatosis (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Multicentric infantile myofibromatosis (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Aggressive systemic infantile myofibromatosis (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital lower lip pits (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Hereditary mucoepithelial dysplasia (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Patent vitelline duct (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Vitelline duct polyp (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Hypertrichosis with congenital macrogingivae (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Vertical alopecia (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Sutural alopecia (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Triangular alopecia (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Congenital pigmented nevus with atypical melanocytic proliferation (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Port-wine stain with associated anomalies (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Port-wine stain with oculocutaneous melanosis (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Aplasia cutis congenita due to underlying malformation (Type 4) (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Aplasia cutis congenita associated with fetus papyraceus (Type 5) (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Aplasia cutis congenita in association with epidermolysis bullosa (Type 6) (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Aplasia cutis congenita due to teratogenic drug (Type 7) (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Aplasia cutis congenita following intra-uterine infection (Type 8) (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Oculocerebrocutaneous syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Midline cervical cleft (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cutaneous lesion resulting from spinal dysraphism (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Port-wine stain associated with spinal dysraphism (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cutaneous lesion resulting from spina bifida (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Rudimentary digit (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Drug-induced epidermolysis bullosa acquisita (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Drug-induced cutis laxa (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Pseudoporphyria due to PUVA therapy |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Hemodialysis-associated pseudoporphyria (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Porphyria-like reaction caused by poison and/or environmental toxin |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Porphyria caused by hexachlorobenzene |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Porphyria caused by chlorinated phenol (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Aplasia cutis in Trisomy 13 syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Aplasia cutis in Chromosome 4 short-arm deletion syndrome (Wolf-Hirschhorn) (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Café-au-lait spots and ring chromosome 11 |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Autosomal chromosomal disorder (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
XXYY syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Poly Y syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Odonto-onycho-dermal dysplasia (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Aplasia cutis in Johanson-Blizzard syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Odontomicronychial ectodermal dysplasia (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Port-wine stain in Rubinstein-Taybi syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cardio-acral-facial syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cardio-facio-cutaneous syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Bitemporal scars with abnormal eyelashes |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Cleft palate lateral synechia syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Facial milia, lobate tongue, lingual and labial frenula syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Hereditary neurocutaneous angiomata (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Lamellar ichthyosis (limited type) (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
X-linked dominant chondrodysplasia punctata of Happle |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Ichthyosis, cerebellar degeneration and hepatosplenomegaly (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Photosensitivity with ichthyosis, brittle hair, impaired intelligence, decreased fertility and short stature syndrome |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Ichthyosis follicularis with alopecia and photophobia (IFAP) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|
Flexural Darier's disease (disorder) |
Occurrence |
False |
Congenital |
Inferred relationship |
Some |
|