Ocular Albinism
Also known as: Nettleship-Falls ocular albinism OA1 ocular albinism type 1 X-linked ocular albinism XLOA
Also known as: Nettleship-Falls ocular albinism OA1 ocular albinism type 1 X-linked ocular albinism XLOA
Also known as: OASD ocular albinism with sensorineural deafness deafness and ocular albinism
Also known as: OM
Also known as: COMA Congenital Oculomotor Apraxia oculomotor apraxia, Cogan type saccade initiation failure, congenital
Also known as: Facio-Auriculo-Vertebral Spectrum FAV First and Second Branchial Arch Syndrome Goldenhar-Gorlin Syndrome OAVS OAV Spectrum Oculo-Auriculo-Vertebral Dysplasia
Also known as: Dento-Oculo-Osseous Dysplasia Oculodentodigital Dysplasia Oculo Dento Digital Dysplasia Oculo-Dento-Osseous Dysplasia ODDD ODD Syndrome ODOD Osseous-Oculo-Dento Dysplasia
Also known as: Cross-McKusick-Breen Syndrome Cross Syndrome Depigmentation-Gingival Fibromatosis-Microphthalmia Kramer Syndrome
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Also known as: Delleman-Oorthuys syndrome Delleman syndrome OCCS OCC syndrome orbital cyst with cerebral and focal dermal malformations
Also known as: brown oculocutaneous albinism minimal pigment oculocutaneous albinism OCA1 OCA1A OCA1B OCA3 OCA4 oculocutaneous albinism type 1B platinum oculocutaneous albinism rufous oculocutaneous albinism temperature-sensitive oculocutaneous albinism tyrosinase-negative oculocutaneous albinism tyrosinase-positive oculocutaneous albinism tyrosinase-related OCA yellow oculocutaneous albinism OCA5 OCA6 OCA7 oculocutaneous albinism type 1A
Also known as: autosomal dominant OPMD autosomal recessive OPMD OPMD
Also known as: NAA10-related neurodevelopmental syndrome
Also known as: ACPO acute colonic pseudo-obstruction colonic pseudo-obstruction Ogilvie's syndrome
Also known as: OCNDS CSNK2A1-related disorder
Also known as: dyschondroplasia enchondromatosis multiple cartilaginous enchondroses multiple enchondromatosis