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Disease	Synonyms	Description	Articles
ovarian benign neoplasm		A female reproductive organ benign neoplasm that i..[+] A female reproductive organ benign neoplasm that is located_in the ovary. [-]
organic acidemia	organic acid metabolism disorder; organic aciduria.. [+] organic acid metabolism disorder; organic aciduria [-]	An amino acid metabolic disorder that disrupts nor..[+] An amino acid metabolic disorder that disrupts normal amino acid metabolism causing a building up of branched-chain amino acids. [-]	1 articles
omodysplasia		An osteochondrodysplasia that is characterized by ..[+] An osteochondrodysplasia that is characterized by severe limb shortening and facial dysmorphism. [-]
Ohdo syndrome	Ohdo blepharophimosis syndrome	A syndrome that is characterized by blepharophimos..[+] A syndrome that is characterized by blepharophimosis, ptosis, dental hypoplasia, hearing impairment and intellectual disability. [-]
Ohdo syndrome, SBBYS variant	Ohdo syndrome, SBBYS Variant; Say-Barber-Biesecker.. [+] Ohdo syndrome, SBBYS Variant; Say-Barber-Biesecker-Young-Simpson syndrome; SBBYSS; blepharophimosis-intellectual disability syndrome, SBBYS type [-]	A Ohdo syndrome that is characterized by blepharop..[+] A Ohdo syndrome that is characterized by blepharophimosis, ptosis and intellectual disability and that has_material_basis_in heterozygous mutation in the KAT6B gene on chromosome 10q22. [-]
oculodentodigital dysplasia	ODD syndrome	A syndrome characterized by craniofacial, neurolog..[+] A syndrome characterized by craniofacial, neurologic, limb and ocular abnormalities. [-]
oral hairy leukoplakia	hairy leukoplakia	A mouth disease characterized by a white patch on ..[+] A mouth disease characterized by a white patch on the side of the tongue with a corrugated or hairy appearance; caused by Epstein-Barr virus. [-]
orofaciodigital syndrome I	orofaciodigital syndrome type I; orofaciodigital s.. [+] orofaciodigital syndrome type I; orofaciodigital syndrome 1; Papillon-Leage-Psaume syndrome [-]	An orofaciodigital syndrome that is characterized ..[+] An orofaciodigital syndrome that is characterized by malformations of the face, oral cavity, and digits, has_material_basis_in X-linked dominant inheritance of the OFD1 gene with lethality in males and is associated with polycystic kidney disease. [-]
omphalocele	omphalocoele	A physical disorder characterized by a defect in t..[+] A physical disorder characterized by a defect in the development of the abdominal wall muscles, resulting in the intestines, liver and other organs to remain outside of the abdomen in a sac. [-]
orofaciodigital syndrome III	Sugarman syndrome	An orofaciodigital syndrome that is characterized ..[+] An orofaciodigital syndrome that is characterized by dysmorphic facies and severe intellectual deficits, and has_material_basis_in autosomal recessive inheritance. [-]
orofaciodigital syndrome IV	OFD4; Baraitser-Burn syndrome	An orofaciodigital syndrome that is characterized ..[+] An orofaciodigital syndrome that is characterized by dysmorphic facies, the development of harmartomas of the tongue, polydactyly and limb dysplasia, has_material_basis_in autosomal recessive inheritance of mutations in the TCTN3 gene. [-]
orofaciodigital syndrome V	orofaciodigital syndrome Thurston type; OFD5; poly.. [+] OFD5; orofaciodigital syndrome Thurston type; polydactyly, postaxial, with median cleft of upper lip [-]	An orofaciodigital syndrome that is characterized ..[+] An orofaciodigital syndrome that is characterized by postaxial polydactyly and median cleft of the upper lip and has_material_basis_in homozygous mutation in the DDX59 gene on chromosome 1q32. [-]
orofaciodigital syndrome VII	OFD7; Whelan syndrome	An orofaciodigital syndrome that is characterized ..[+] An orofaciodigital syndrome that is characterized by oral, facial and digital abnormalities, and has_material_basis_in autosomal dominant inheritance. [-]
orofaciodigital syndrome VIII	OFD8; Edwards syndrome	An orofaciodigital syndrome that is characterized ..[+] An orofaciodigital syndrome that is characterized by tongue lobulation, hypoplasia of the epiglottis, cleft lip, polydactyly, short stature and intellectual deficit, and has_material_basis_in X-linked recessive inheritance. [-]
orofaciodigital syndrome X	orofaciodigital syndrome with fibular aplasia; OFD.. [+] orofaciodigital syndrome with fibular aplasia; OFD10 [-]	An orofaciodigital syndrome that is characterized ..[+] An orofaciodigital syndrome that is characterized by facial, oral and digital deformities as well as radial shortening, fibular agenesis and coalescence of tarsal bones. [-]
orofaciodigital syndrome XI		An orofaciodigital syndrome that is characterized ..[+] An orofaciodigital syndrome that is characterized by blepharophimosis, bulbous nasal tip, broad nasal bridge, downslanting palpebral fissures, low set ears, skeletal malformations, intellectual deficits, deafness and congenital heart defects. [-]
orofaciodigital syndrome IX	orofaciodigital syndrome with retinal abnormalitie.. [+] orofaciodigital syndrome with retinal abnormalities; OFD9 [-]	An orofaciodigital syndrome that is characterized ..[+] An orofaciodigital syndrome that is characterized by highly arched palate with bifid tongue, harmartomatous tongue, hypertelorism, telecanthus, strabismus, bifid nasal tip, short stature, bifid halluces, forked metatarsal, polydactyly, mild intellectual deficit and specific retinal abnormalities, and has_material_basis_in autosomal recessive inheritance. [-]
oculoauricular syndrome		A syndrome characterized by microcornea, microphth..[+] A syndrome characterized by microcornea, microphthalmia, anterior-segment dysgenesis, cataract, coloboma of various parts of the eye, abnormalities of the retinal pigment epithelium, and rod-cone dystrophy and a particular cleft ear lobule. [-]
orange allery	Citrus sinensis fruit allergy	A fruit allergy triggered by Citrus sinensis plant..[+] A fruit allergy triggered by Citrus sinensis plant fruit food product. [-]
osteoporosis-pseudoglioma syndrome	ocular form of osteogenesis imperfecta; OPPG	A syndrome characterized by congenital or infancy-..[+] A syndrome characterized by congenital or infancy-onset blindness, very low bone mass, decreased trabecular bone volume, severe juvenile-onset osteoporosis and spontaneous fractures, pseudoglioma, microphthalmia that has_material_basis_in homozygous or compound heterozygous mutation in the LRP5 gene on chromosome 11q13. [-]

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