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Diseases
Genes (350)
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GJA1
Oculodentodigital Dysplasia
MYO5B
Microvillus Inclusion Disease
COL7A1
Generalized Dominant Dystrophic Epidermolysis Bullosa
FGF10
Aplasia Of Lacrimal And Salivary Glands
MC2R
Familial Glucocorticoid Deficiency
ATR
Cutaneous Telangiectasia And Cancer Syndrome, Familial
ALPL
Odontohypophosphatasia
COX4I2
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis
STX3
Microvillus Inclusion Disease
MRAP
Familial Glucocorticoid Deficiency
MBTPS2
Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant
MMP20
Early Childhood Caries
Dental Fluorosis
Amelogenesis Imperfecta, Hypomaturation Type, Iia1
STAR
Adrenal Crisis
Familial Glucocorticoid Deficiency
SAT1
Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant
SART3
Disseminated Superficial Actinic Porokeratosis
PTCH1
Oculodentodigital Dysplasia
PTCH2
Oculodentodigital Dysplasia
SUFU
Oculodentodigital Dysplasia
KLK4
Early Childhood Caries
Amelogenesis Imperfecta, Hypomaturation Type, Iia1
LRP1
Keratosis Follicularis Spinulosa Decalvans, Autosomal Dominant