IGDRPT (Indian Genetic Disease Risk Prediction Tool)
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IGDRPT
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Select Gene Name
Please Select Gene Name
FGFR3
AAAS
AR
PAX6
RYR2
TCIRG1
DMD
HBB
BTD
HRAS
CFTR
CTNS
SLC4A1
ASAH1
UGT1A1
G6PC
SLC29A3
FVIII
FGB
NEMO
GJB2
TYR
CTSC
PROC
MECP2
ATP7B
BTK
- OR -
Select Disease Name
Please Select Disease Name
Achondroplasia
Allgrove syndrome
Androgen insensitivity syndrome
Aniridia
Arrhythmogenic right ventricular dysplasia
Autosomal recessive infantile malignant osteopetrosis
Becker Muscular Dystrophy
Beta Thalassemia
Biotidinase Deficiency
Costello Syndrome
Cystic Fibrosis
Cystinosis nephropathic
Distal renal tubular acidosis
Farber lipogranulomatosis
Gilbert Syndrome
Glycogen storage disease Ia
H syndrome
Haemophilia A
Hypofibrinogenemia
Incontinetia pigmenti
Non-syndromic Hearing Loss (DFNB1A)
Oculocutaneous Albinism type 1 (OCA1)
Papillon-Lefevre syndrome
Purpura
Rett Syndrome
Wilson Disease (WD)
X-linked agammaglobulinemia
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Browse by mode of inheritance
Autosomal Dominant
Autosomal Recessive
X-linked Recessive
X-linked Dominants
Inheritance: X-linked Dominants
Rett Syndrome
