Western Australian Consolidated Regulations[Reg. 10(1)]
Category 1.
Conditions in which
the evidence for inheritance is conclusive.
Abnormalities of
mesonephric duct development
Abnormalities of
paramesonephric duct development (in female progeny)
Abortion due to lethal
mutation
Acantholysis, familial
Anchondroplasia and
dwarfism of all types
Agnathia
Albinism
Alopecia
Ankylosis
Arthrogryposis and
cleft palate
Ataxia, neonatal with
leucodysplasia
Brain oedema,
congenital
Bulldog Calf
Cataract
Cerebellar hypoplasia
Cerebral hernia
Chromosomal
translocation and other chromosomal abnormalities
Cleft palate and hair
lip
Coloboma
Convulsions and
ataxia, familial
Cryptorchidism
Cystic ovaries (in
female progeny)
Dermal aplasia
Dropsy, congenital
Dystocia, high
incidence in female progeny
Ectromelia
Epilepsy
Epitheliogenesis
imperfecta
Exophthalmos with
strabismus
Gestation, prolonged
Hermaphroditism
Hip dysplasia and
degenerative arthropathy
Hydrocephalus
Hypotrichosis
Ichthyosis
Inability to serve,
specific defects
Inguinal hernia
Libido, primary lack
of or reduced
Lymphatic obstruction
Mannosidosis
(pseudolipidosis)
Microencephaly
Muscular hypertrophy,
double muscling
Ocular defects,
multiple
Osteopetrosis
Ovarian hypoplasia (in
female progeny)
Paresis
Penis, short
Periodic Spasticity
Polydactylism
Porphyria
Posterior paralysis
Probatocephalie
(Sheeps Head)
Prognathism
Spasms, congenital
Sperm, specific
morphological defects
Spermiostasis
Spondylarthrosis,
deforming
Syndactylism
Tail defects
Tendon contracture,
multiple
Umbilical hernia
Category 2.
Conditions in which
the evidence for inheritance is not conclusive:
Pendulous prepuce and
preputial prolapse
Penile deviations
Persistent frenulum of
penis
Spondylitis and other
forms of degenerative arthropathy
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