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Agenesis of the Diaphragm
Diaphragmatic Hernia, Congenital
Hypopigmentation
Incontinentia pigmenti
Retinitis pigmentosa
Albinism, Minimal Pigment Type
Amelogenesis Imperfecta Pigmented Hypomaturation Type
Anterior Segment Mesenchymal Dysgenesis
Asternia with Cardiac, Diaphragmatic, and Abdominal Defects
Cataract, Microphthalmia and Nystagmus
Cholestasis Pigmentary Retinopathy Cleft Palate
Chorea, Remitting with Nystagmus and Cataracts
Chronic Demyelinizing Neuropathy with IgM Monoclonal
Congenital Diaphragmatic Hernia
Corneal Dystrophy Pigmentary Anomaly Malabsorption
Dandy-Walker Malformation with Nasopharyngeal Teratoma and Diaphragmatic Hernia
Dermatopathia Pigmentosa Reticularis
Diaphragmatic Agenesia
Diaphragmatic Agenesis Radial Aplasia Omphalocele
Diaphragmatic Defect Limb Deficiency Skull Defect
Diaphragmatic Hernia Exomphalos Corpus Callosum Agenesis
Diaphragmatic Hernia Upper Limb Defects
Dwarfism Deafness Retinitis Pigmentosa
Dyssegmental Dysplasia and Glaucoma
Dyssegmental Dysplasia Rolland-Desbuquois Type
Dyssegmental Dysplasia Silverman-Handmaker Type
Epidermolysis Bullosa Simplex with Mottled Pigmentation
Episodic Ataxia with Nystagmus
Epitheliopathy, Acute Posterior Multifocal Placoid Pigment
Extrasystoles Short Stature Hyperpigmentation Microcephaly
Focal Segmental Glomerulosclerosis
Gangliosidosis Generalized GM1 Type 1
Gangliosidosis GM1 Type 3
Gangliosidosis, Generalized GM1 Type 2
Giant Pigmented Hairy Nevus
GM2 Gangliosidosis, 0 Variant
GM2-Gangliosidosis, B, B1, AB Variant
Gms Syndrome
Hydrocephaly corpus callosum agenesis diaphragmatic hernia
Hypogonadism retinitis pigmentosa
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response
Immunodeficiency with hyper IgM type 1
Immunodeficiency with hyper IgM type 2
Immunodeficiency with hyper IgM type 3
Immunodeficiency with hyper IgM type 4
Immunodeficiency with hyper IgM type 5
Lumbar malsegmentation short stature
Macules hereditary congenital hypopigmented and hyperpigmented
Mental retardation hypotonia skin hyperpigmentation
Microcephaly cardiac defect lung malsegmentation
Microphthalmia diaphragmatic hernia Fallot
Mirror polydactyly segmentation and limbs defects
Muscular atrophy ataxia retinitis pigmentosa and diabetes mellitus
Myxoma-spotty pigmentation-endocrine overactivity
Neuropathy ataxia retinitis pigmentosa syndrome
Nevus of ota retinitis pigmentosa
Nystagmus 1, congenital, X- linked
Nystagmus 2, congenital, autosomal dominant
Nystagmus 3, congenital, autosomal dominant
Nystagmus 4, congenital, autosomal dominant
Nystagmus, congenital motor, autosomal recessive
Nystagmus, hereditary vertical
Nystagmus, myoclonic
Oculocerebral hypopigmentation syndrome type Preus
Oculocerebral syndrome with hypopigmentation
Osteopathia striata with pigmentary dermopathy including white forelock
Osteoporosis oculocutaneous hypopigmentation syndrome
Patterned dystrophy of retinal pigment epithelium
Phacomatosis pigmentokeratotica
Phacomatosis pigmentovascularis
Pigment-dispersion syndrome
Pigmentary retinopathy
Pigmented purpuric eruption
Pigmented villonodular synovitis
Polyposis skin pigmentation alopecia fingernail changes
Posterior column ataxia with retinitis pigmentosa
Progeroid short stature with pigmented nevi
Progressive black carbon hyperpigmentation of infancy
Punctate acrokeratoderma freckle like pigmentation
Radioulnar synostosis retinal pigment abnormalities
Rectosigmoid neoplasm
Red skin pigment anomaly of New Guinea
Renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia
Retinis pigmentosa deafness hypogenitalism
Retinitis pigmentosa 1
Retinitis Pigmentosa 11
Retinitis pigmentosa 12
Retinitis Pigmentosa 13
Retinitis Pigmentosa 14
Retinitis Pigmentosa 15
Retinitis Pigmentosa 17
Retinitis Pigmentosa 18
Retinitis Pigmentosa 19
Retinitis pigmentosa 2, x linked
Retinitis Pigmentosa 20
Retinitis Pigmentosa 22
Retinitis Pigmentosa 23
Retinitis Pigmentosa 24
Retinitis Pigmentosa 25
Retinitis Pigmentosa 26

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See National Library of Medicine Resources for GM