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Preimplantation genetic diagnosis (PGD) was developed specifically for the identification of embryos with genetic abnormalities.

Sydney IVF has developed tests for more than 115 inherited diseases.

 ConditionSorted By Condition In Ascending Order
ABO blood type incompatability
Alagille syndrome
Alpers disease
alpha 1 anti-trypsin
alpha-thalassemia
Alport syndrome
anti-Kell antibodies
Becker muscular dystrophy
beta-thalassemia
blepharophimosis ptosis epicanthus inversus
breast cancer, gene 1
breast cancer, gene 2
carbamoyl phosphate synthetase deficiency
central core disease
cerebral arteriopathy (Cadasil)
Charcot-Marie-Tooth syndrome 1A
Charcot-Marie-Tooth syndrome 1B
chronic granulomatosis disease (CGD)
congenital adrenal hyperplasia
congenital disorder of glycosylation
congenital nephrotic syndrome
connexin 26
Crigler-Najjar syndrome I
Crouzon syndrome
cystic fibrosis
Czech dysplasia
Dejerine-Sottas syndrome
Duchenne muscular dystrophy
early onset Alzheimer disease
early onset torsion dystonia
E-cadherin
ectodermal dysplasia
Emery Dreifuss muscular dystrophy
epidermolysis bullosa, dominant dystrophic
epidermolysis bullosa, Herlitz junctional, gene 1
epidermolysis bullosa, Herlitz junctional, gene 2
epidermolytic palmoplantar keratosis
facioscapulohumeral muscular dystrophy
familial adenomatous polyposis
familial amytrophic lateral sclerosis (Lou Gehrig's disease)
Fechtner syndrome
fragile X
fumarase deficiency
galactosemia
Gaucher disease type 2
glucose-6-phosphate dehydrogenase
Goldberg-Shprintzen syndrome
Gorlin syndrome
haemophilia A
haemophilia B
hereditary non polyposis colon cancer 2
hereditary spherocytosis
Hirschsprung's disease
HLA match for Wiskott-Aldrich syndrome
HLA match with beta thalassemia
HLA match with diamond blackfan anemia
HLA match with hyper IgM
HLA match with sickle cell anemia
HLA matching
Holt Oram Syndrome
Hunter syndrome (mucopolysaccharidosis II A)
Huntington disease
Hyper IgM
hypochondroplasia
hypophosphatasia
hypophosphatemic rickets
incontinentia pigmenti
infantile neuroaxonal dystrophy
juvenile neuronal ceroid lipofuscinosis
juvenile retinoschisis
late infantile neuronal ceroid lipofuscinosis(Batten disease)
Lowe oculocerebrorenal syndrome
medium-chain acyl-CoA dehydrogenase deficiency
medullary thyroid carcinoma (RET)
metachromatic leukodystrophy
mucopolysaccharidosis III B
multiple endocrine neoplasia 2A
multiple hereditary exotoses
myotonic muscular dystrophy
myotubular myopathy
nail-patella syndrome
nemaline myopathy
nephrogenic diabetes insipidus
neurofibromatosis types 1
neurofibromatosis types 2
Norrie disease
oculocutaneous albinism
ornitrine transcarbamylase deficiency
osteogenesis imperfecta type 1
palmoplantar hyperkeratosis
Pendred syndrome
pericentric inversion of X
polycystic kidney disease, autosomal dominant, gene 1
polycystic kidney disease, autosomal dominant, gene 2
polycystic kidney disease, autosomal recessive
proximal myotonic myopathy
psoriasis, susceptibility gene
pulmonary alveolar proteinosis
retinoblastoma
rhesus D disease
Saethre-Chotzen syndrome
Sandhoff disease
sickle-cell anaemia
Simpson Golabi Behmel syndrome
spastic paraplegia
spinal muscular atrophy 1
spinal muscular atrophy 2
spinal muscular atrophy 3
Stickler syndrome
thyroid cancer
translocations - various
transthyretin amyloidosis
Treacher-Collins syndrome
tuberous sclerosis, gene 1
tuberous sclerosis, gene 2
Ullrich congenital muscular dystrophy
vitelliform macular dystrophy
von Hippel-Lindau disease
Wilms tumour
Wiskott-Aldrich syndrome
Wolman disease
X-linked adrenoleukodystrophy
X-linked choroideremia
Zellweger syndrome