Abnormality of the pulmonary artery, Abnormality of vision, Aganglionic megacolon, Albinism, Bilateral sensorineural hearing impairment, Blue irides, Coloboma, Congenital sensorineural hearing impairment, Constipation, Cutaneous melanoma, Frontal bossing, Generalized hypopigmentation, Generalized hypotonia, Giant melanosomes in melanocytes, Hearing impairment, Heterochromia iridis, Hypermetropia, Hypopigmentation of hair, Hypopigmentation of the fundus, Hypopigmentation of the skin, Hypopigmented skin patches, Hypoplasia of the fovea, Hypoplastic iris stroma, Intestinal obstruction, Macrocephaly, Micrognathia, Microphthalmia, Multiple lentigines, Nystagmus, Ocular albinism, Olfactory lobe agenesis, Optic nerve dysplasia, Osteopetrosis, Partial albinism, Photophobia, Posteriorly rotated ears, Preauricular pit, Premature graying of hair, Prominent nasal bridge, Ptosis, Reduced visual acuity, Renal cell carcinoma, Sensorineural hearing impairment, Shallow orbits, Strabismus, Synophrys, Telecanthus, Underdeveloped nasal alae, Vestibular hypofunction, Visual impairment, White eyebrow, White eyelashes, White forelock, Wide nasal bridge

abnormal eye size, abnormal fertility/fecundity, abnormal foot pigmentation, abnormal hair follicle melanocyte morphology, abnormal hair follicle morphology, abnormal hair shaft melanin granule morphology, abnormal hearing physiology, abnormal iris stromal pigmentation, abnormal long bone epiphyseal plate morphology, abnormal long bone metaphysis morphology, abnormal melanoblast migration, abnormal melanoblast morphology, abnormal melanocyte morphology, abnormal nursing, abnormal optic choroid morphology, abnormal optic cup morphology, abnormal optic fissure closure, abnormal optic stalk morphology, abnormal osteoclast morphology, abnormal osteoclast physiology, abnormal photoreceptor inner segment morphology, abnormal pinna reflex, abnormal retina development, abnormal retina neuronal layer morphology, abnormal retina photoreceptor morphology, abnormal retina pigment epithelium morphology, abnormal rod electrophysiology, abnormal scala media morphology, abnormal spleen germinal center morphology, abnormal spleen red pulp morphology, abnormal spleen white pulp morphology, abnormal stria vascularis morphology, abnormal vitreous body morphology, absent coat pigmentation, absent eye pigmentation, absent hair follicle melanin granules, absent photoreceptor outer segment, absent pinna reflex, absent retina cone cells, absent retina rod cells, absent strial intermediate cells, belly spot, darkened coat color, decreased bleeding time, decreased body size, decreased ear pigmentation, decreased eye pigmentation, decreased litter size, decreased mast cell number, decreased melanocyte number, decreased osteoclast cell number, decreased serotonin level, decreased survivor rate, decreased tail pigmentation, diluted coat color, eyelids fail to open, fetal growth retardation, head spot, increased or absent threshold for auditory brainstem response, increased osteoclast cell number, increased trabecular bone connectivity density, increased width of hypertrophic chondrocyte zone, irregular coat pigmentation, no abnormal phenotype detected, non-pigmented tail tip, osteosclerosis, phenotypic reversion, pigmentation phenotype, postnatal lethality, premature death, reduced fertility, retina photoreceptor degeneration, skeleton phenotype, thin stria vascularis, vacuolated lens, variegated coat color, vision/eye phenotype, white spotting, yellow coat color