Aganglionic megacolon, Anemia, Angioedema, Anorexia, Arrhythmia, Asthma, Ataxia, Azoospermia, Carcinoma, Cardiorespiratory arrest, Choriocarcinoma, Chronic leukemia, Chronic myelogenous leukemia, Chronic myelomonocytic leukemia, Constipation, Cough, Cryptorchidism, Cutaneous mastocytosis, Diarrhea, Dysphagia, Edema, Eosinophilia, Erythema, Erythroderma, Esophageal neoplasm, Fatigue, Gastrointestinal hemorrhage, Gastrointestinal stroma tumor, Gonadal dysgenesis, Headache, Hearing impairment, Hepatomegaly, Heterochromia iridis, Hypercalcemia, Hypermelanotic macule, Hyperpigmentation of the skin, Hypopigmentation of hair, Hypopigmented skin patches, Hypotension, Hypotonia, Immunologic hypersensitivity, Impaired temperature sensation, Intellectual disability, Intestinal obstruction, Irregular hyperpigmentation, Large hands, Long philtrum, Macule, Mastocytosis, Microcephaly, Myelodysplasia, Nausea and vomiting, Neoplasm, Neoplasm of the colon, Neoplasm of the gastrointestinal tract, Neoplasm of the rectum, Neoplasm of the skin, Neoplasm of the small intestine, Neoplasm of the stomach, Neurofibromas, Non-Hodgkin lymphoma, Osteoporosis, Partial albinism, Piebaldism, Profuse pigmented skin lesions, Pruritus, Recurrent fractures, Respiratory insufficiency, Sarcoma, Skin rash, Splenomegaly, Subcutaneous nodule, Synophrys, Telangiectasia macularis eruptiva perstans, Telangiectasia of the skin, Teratoma, Thickened skin, Urticaria, White eyebrow, White eyelashes, White forelock, Wide nasal bridge

abnormal cochlear outer hair cell morphology, abnormal definitive hematopoiesis, abnormal digestive system morphology, abnormal ear pigmentation, abnormal erythrocyte cell number, abnormal erythroid progenitor cell morphology, abnormal erythropoiesis, abnormal eye pigmentation, abnormal feces composition, abnormal female germ cell morphology, abnormal female reproductive system morphology, abnormal foot pigmentation, abnormal interferon level, abnormal interleukin level, abnormal interstitial cell of Cajal morphology, abnormal melanoblast migration, abnormal melanoblast morphology, abnormal melanocyte morphology, abnormal melanosome morphology, abnormal myenteric nerve plexus morphology, abnormal oocyte morphology, abnormal organ of Corti morphology, abnormal otolith morphology, abnormal ovarian follicle morphology, abnormal ovarian follicle number, abnormal ovarian folliculogenesis, abnormal primordial germ cell migration, abnormal primordial germ cell morphology, abnormal primordial ovarian follicle morphology, abnormal proerythroblast morphology, abnormal renal glomerulus morphology, abnormal response to cardiac infarction, abnormal response to transplant, abnormal response/metabolism to endogenous compounds, abnormal seminiferous tubule morphology, abnormal spermatogonia proliferation, abnormal stria vascularis morphology, abnormal stria vascularis vasculature morphology, abnormal strial basal cell morphology, abnormal strial marginal cell morphology, abnormal survival, abnormal tectorial membrane morphology, abnormal vascular permeability, abnormal ventral coat pigmentation, absent coat pigmentation, absent endocochlear potential, absent oocytes, absent ovarian follicles, absent strial intermediate cells, arrest of spermatogenesis, arrested B cell differentiation, asthenozoospermia, belly blaze, belly spot, belted, cochlear ganglion degeneration, cochlear hair cell degeneration, constricted vagina orifice, crypts of Lieberkuhn abscesses, deafness, decreased Cajal-Retzius cell number, decreased airway responsiveness, decreased bone marrow cell number, decreased ear pigmentation, decreased epididymis weight, decreased erythrocyte cell number, decreased fetal size, decreased hematocrit, decreased hemoglobin content, decreased litter size, decreased male germ cell number, decreased mast cell degranulation, decreased mast cell number, decreased mean corpuscular volume, decreased physiological sensitivity to xenobiotic, decreased primordial germ cell proliferation, decreased survivor rate, decreased susceptibility to induced arthritis, decreased susceptibility to type I hypersensitivity reaction, decreased tail pigmentation, decreased testis weight, decreased thymocyte number, decreased tumor growth/size, decreased vascular permeability, delayed female fertility, digestive/alimentary phenotype, diluted coat color, distended cecum, distended ileum, distended stomach, embryonic lethality before implantation, complete penetrance, embryonic lethality during organogenesis, complete penetrance, embryonic lethality during organogenesis, incomplete penetrance, embryonic lethality, complete penetrance, enlarged cecum, enlarged otoliths, glomerular crescent, growth/size/body region phenotype, head blaze, head spot, hearing/vestibular/ear phenotype, hematopoietic system phenotype, high mean erythrocyte cell number, homeostasis/metabolism phenotype, hyperpigmentation, immune system phenotype, impaired behavioral response to xenobiotic, impaired neutrophil recruitment, impaired ovarian folliculogenesis, increased erythroblast number, increased erythrocyte cell number, increased erythrocyte protoporphyrin level, increased esophageal papilloma incidence, increased gastrointestinal tumor incidence, increased mast cell degranulation, increased mean corpuscular hemoglobin, increased mean corpuscular hemoglobin concentration, increased myocardial infarct size, increased nucleated erythrocyte cell number, increased or absent threshold for auditory brainstem response, increased papilloma incidence, increased physiological sensitivity to xenobiotic, increased sensitivity to induced morbidity/mortality, increased sensitivity to xenobiotic induced morbidity/mortality, increased skin tumor incidence, increased susceptibility to parasitic infection, increased tumor growth/size, interstitial cells of Cajal hyperplasia, irregular coat pigmentation, lethality at weaning, incomplete penetrance, lethality throughout fetal growth and development, complete penetrance, lethality, incomplete penetrance, low mean erythrocyte cell number, macrocytosis, meteorism, neonatal lethality, complete penetrance, neonatal lethality, incomplete penetrance, non-pigmented tail tip, organ of Corti degeneration, ovary hyperplasia, perinatal lethality, complete penetrance, perinatal lethality, incomplete penetrance, pigmentation phenotype, postnatal lethality, postnatal lethality, complete penetrance, postnatal lethality, incomplete penetrance, premature death, prenatal lethality, prenatal lethality, complete penetrance, prenatal lethality, incomplete penetrance, preweaning lethality, incomplete penetrance, reduced female fertility, reduced fertility, reduced male fertility, reproductive system phenotype, reversion by mitotic recombination, slow postnatal weight gain, small cecum, small intestinal inflammation, small ovary, spleen hyperplasia, testis hypoplasia, thin stria vascularis, vestibular hair cell degeneration, white spotting