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Dilution, Pigmentary
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Acanthosis Nigricans
Acrocephalopolydactylous Dysplasia
Albinism
Albinism, Oculocutaneous, Type Ii
Alopecia
Al-Raqad Syndrome
Amelanotic Melanoma
Angelman Syndrome
Aniridia 1
Anorectal Anomalies
Anorexia Nervosa 1
Anterior Uveitis
Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus
Basal Cell Carcinoma
Blood Group--Ahonen
Burns
Burn Scar
Cataract
Charcot-Marie-Tooth Disease
Chediak-Higashi Syndrome
Choroiditis
Cole Disease
Congenital Nystagmus
Dowling-Degos Disease
Erythema Multiforme
Familial Progressive Hyperpigmentation
Frontal Fibrosing Alopecia
Griscelli Syndrome
Hereditary Spastic Paraplegia
Hermansky-Pudlak Syndrome
Heterochromia Iridis
Homocystinuria
Homocystinuria Due to Cystathionine Beta-Synthase Deficiency
Hyperpigmentation with or Without Hypopigmentation, Familial Progressive
Hypertrichosis
Hypomelanotic Disorder
Hypotonia
Kallmann Syndrome
Keratosis
Lichen Sclerosus
Melanoma
Microcephaly
Microphthalmia
Moebius Syndrome
Mycosis Fungoides
Neuropathy
Night Blindness
Ocular Albinism
Oculocerebral Hypopigmentation Syndrome of Preus
Oculocerebral Syndrome with Hypopigmentation
Oculocutaneous Albinism
Pallister-Killian Mosaic Syndrome
Pallister-Killian Syndrome
Papillary Carcinoma
Paraplegia
Peroneal Neuropathy
Phenylketonuria
Piebald Trait
Pityriasis Lichenoides
Pityriasis Lichenoides Chronica
Pityriasis Lichenoides Et Varioliformis Acuta
Ptosis
Pulmonary Alveolar Microlithiasis
Punctate Palmoplantar Keratoderma
Raindrop Hypopigmentation
Spasticity
Squamous Cell Carcinoma
Storage Pool Platelet Disease
Superficial Basal Cell Carcinoma
Tenosynovitis
Thyroiditis
Tietz Albinism-Deafness Syndrome
Tooth Disease
Uveitis
Vici Syndrome
Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6
Waardenburg's Syndrome
Waardenburg Syndrome, Type 1
Waardenburg Syndrome, Type 2e
Waardenburg Syndrome, Type 4c
Yemenite Deaf-Blind Hypopigmentation Syndrome
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