rs1131692034, EDA

N. diseases: 14
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Peg-shaped teeth
CUI: C0266037
Disease: Peg-shaped teeth
0.700 CausalMutation CLINVAR
Periorbital hyperpigmentation
CUI: C1844606
Disease: Periorbital hyperpigmentation
0.700 CausalMutation CLINVAR
Hypodontia
CUI: C0020608
Disease: Hypodontia
0.700 CausalMutation CLINVAR
Depressed nasal bridge
CUI: C1836542
Disease: Depressed nasal bridge
0.700 CausalMutation CLINVAR
Brittle hair
CUI: C0263490
Disease: Brittle hair
0.700 CausalMutation CLINVAR
Christ-Siemens-Touraine syndrome
CUI: C0162359
Disease: Christ-Siemens-Touraine syndrome
0.700 CausalMutation CLINVAR
Diminished sweating
CUI: C0553721
Disease: Diminished sweating
0.700 CausalMutation CLINVAR
Anhydrotic Ectodermal Dysplasias
CUI: C1706004
Disease: Anhydrotic Ectodermal Dysplasias
0.700 CausalMutation CLINVAR
Frontal bossing
CUI: C0221354
Disease: Frontal bossing
0.700 CausalMutation CLINVAR
Thin skin
CUI: C0423757
Disease: Thin skin
0.700 CausalMutation CLINVAR
Sparse and thin eyebrow
CUI: C4282407
Disease: Sparse and thin eyebrow
0.700 CausalMutation CLINVAR
Congenital hypotrichia
CUI: C4721530
Disease: Congenital hypotrichia
0.700 CausalMutation CLINVAR
Dry skin
CUI: C0151908
Disease: Dry skin
0.700 CausalMutation CLINVAR
Sparse eyelashes
CUI: C1843300
Disease: Sparse eyelashes
0.700 CausalMutation CLINVAR