Experimental Factor Ontology
4217 terms(s) returned
| Term Type: | Record: 1 to 50 of 4217 Records | Page: 1 of 85, First Previous Next Last | Show Records Per Page |
- Obesity - colitis - hypothyroidism - cardiac hypertrophy - developmental delay
- Obesity due to MC3R deficiency
- Obesity due to congenital leptin resistance
- Ocular albinism with congenital sensorineural deafness
- Oculo-oto-facial dysplasia
- Oculoauricular syndrome, Schorderet type
- Oculomotor apraxia or related oculomotor disease
- Oculomotor palsy
- Odonto-onycho dysplasia - alopecia
- Odontomatosis - aortae esophagus stenosis
- Okihiro syndrome
- Oley syndrome
- Oligodontia - cancer predisposition syndrome
- Olivopontocerebellar atrophy - deafness
- Ondine syndrome
- Onycho-patellar syndrome with eye involvement
- Ophthalmoplegia - intellectual disability - lingua scrotalis
- Optic atrophy-intellectual disability syndrome
- Optic neuropathy
- Organic aciduria
- Orofaciodigital syndrome type 1
- Orofaciodigital syndrome type 10
- Orofaciodigital syndrome type 11
- Orofaciodigital syndrome type 2
- Orofaciodigital syndrome type 3
- Orofaciodigital syndrome type 4
- Orofaciodigital syndrome type 5
- Orofaciodigital syndrome type 8
- Orofaciodigital syndrome type 9
- Ossification anomalies - psychomotor development delay
- Osteochondrodysplatic nanism - deafness - retinitis pigmentosa
- Osteodysplasty, Melnick-Needles type
- Osteogenesis imperfecta - retinopathy - seizures - intellectual disability
- Osteopathia striata - cranial sclerosis
- Osteopathia striata - pigmentary dermopathy - white forelock
- Osteopenia - myopia - hearing loss - intellectual disability - facial dysmorphism
- Osteopetrosis - hypogammaglobulinemia
- Osteopetrosis with renal tubular acidosis
- Osteoporosis - macrocephaly - blindness - joint hyperlaxity
- Osteoporosis - oculocutaneous hypopigmentation syndrome
- Osteoporosis - pseudoglioma
- Osteosclerosis - ichthyosis - premature ovarian failure
- Other genetic epidermal disease
- Other immunodeficiency syndrome with predominantly antibody defects
- Other immunodeficiency syndromes due to defects in innate immunity
- Other metabolic disease
- Other syndrome with lissencephaly as a major feature
- Otomandibular dysplasia associated with monogenic syndromes
- Overgrowth - macrocephaly - facial dysmorphism
- obsolete_10q22.3q23.3 microdeletion syndrome
