WA 0821 7001 0763 (FORTRESS) Pintu Rumah Cluster Harga Terbaik Depati Vii Kerinci Jambi

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COL7A1
- Epidermolysis Bullosa Acquisita
- Transient Bullous Dermolysis Of The Newborn
- Dystrophic Epidermolysis Bullosa
- Pretibial Dystrophic Epidermolysis Bullosa
- Epidermolysis Bullosa Dystrophica, Autosomal Recessive
- Acral Dystrophic Epidermolysis Bullosa
- Centripetalis Recessive Dystrophic Epidermolysis Bullosa
- Dystrophic Epidermolysis Bullosa Pruriginosa
- Epidermolysis Bullosa Dystrophica
- Epidermolysis Bullosa With Congenital Localized Absence Of Skin And Deformity Of Nails
- Epidermolysis Bullosa Simplex Superficialis
COL1A2
- Osteogenesis Imperfecta, Type Vii
- Ehlers-Danlos Syndrome, Dermatosparaxis Type
- Ehlers-Danlos Syndrome, Arthrochalasia Type, 2
COL1A1
- Osteogenesis Imperfecta, Type Vii
- Epidermolysis Bullosa Dystrophica
- Ehlers-Danlos Syndrome, Arthrochalasia Type, 2
VKORC1
- Hereditary Combined Deficiency Of Vitamin K-Dependent Clotting Factors
- Coumarin Resistance
- Vitamin K Deficiency
GALE
- Galactose Epimerase Deficiency
- Galactose-1-Phosphate Uridylyltransferase Deficiency
GALT
- Galactose Epimerase Deficiency
- Galactose-1-Phosphate Uridylyltransferase Deficiency
ATRX
- Alpha-Thalassemia Mental Retardation Syndrome
GUSB
- Mucopolysaccharidosis Type Vii
- Haemophilia A
F12
- Factor Xii Deficiency
F8
- Hereditary Combined Deficiency Of Vitamin K-Dependent Clotting Factors
- Vitamin K Deficiency
- Haemophilia A
MMP1
- Epidermolysis Bullosa Acquisita
- Epidermolysis Bullosa Dystrophica, Autosomal Recessive
- Dystrophic Epidermolysis Bullosa Pruriginosa
- Epidermolysis Bullosa Dystrophica
PFKM
- Glycogen Storage Disease Vii
HOXA1
- Athabaskan Brainstem Dysgenesis Syndrome
F7
- Factor Vii Deficiency
- Vitamin K Deficiency
- Haemophilia A
F9
- Factor Vii Deficiency
- Coumarin Resistance
- Haemophilia A
GGCX
- Hereditary Combined Deficiency Of Vitamin K-Dependent Clotting Factors
- Vitamin K Deficiency
ADAMTS2
- Ehlers-Danlos Syndrome, Dermatosparaxis Type
GALK1
- Galactose Epimerase Deficiency
- Galactose-1-Phosphate Uridylyltransferase Deficiency
LRMDA
- Albinism, Oculocutaneous, Type Vii
PCDH19
- Epilepsy-Intellectual Disability In Females