Experimental Factor Ontology
6843 terms(s) returned
| Term Type: | Record: 2301 to 2350 of 6843 Records | Page: 47 of 137, First Previous Next Last | Show Records Per Page |
- Autosomal dominant multiple pterygium syndrome
- Autosomal dominant nail dysplasia
- Autosomal dominant optic atrophy and cataract
- Autosomal dominant optic atrophy and late-onset deafness
- Autosomal dominant optic atrophy, classic type
- Autosomal dominant osteopetrosis type 1
- Autosomal dominant primary hypomagnesemia with hypocalciuria
- Autosomal dominant spastic paraplegia type 10
- Autosomal dominant spastic paraplegia type 12
- Autosomal dominant spastic paraplegia type 13
- Autosomal dominant spastic paraplegia type 17
- Autosomal dominant spastic paraplegia type 19
- Autosomal dominant spastic paraplegia type 29
- Autosomal dominant spastic paraplegia type 3
- Autosomal dominant spastic paraplegia type 31
- Autosomal dominant spastic paraplegia type 36
- Autosomal dominant spastic paraplegia type 37
- Autosomal dominant spastic paraplegia type 38
- Autosomal dominant spastic paraplegia type 4
- Autosomal dominant spastic paraplegia type 41
- Autosomal dominant spastic paraplegia type 42
- Autosomal dominant spastic paraplegia type 6
- Autosomal dominant spastic paraplegia type 8
- Autosomal dominant striatal neurodegeneration
- Autosomal ichthyosis syndrome with fatal disease course
- Autosomal ichthyosis syndrome with other associated signs
- Autosomal ichthyosis syndrome with prominent hair abnormalities
- Autosomal ichthyosis syndrome with prominent neurologics signs
- Autosomal monosomy
- Autosomal recessive Charcot-Marie-Tooth disease with hoarseness
- Autosomal recessive axonal neuropathy with neuromyotonia
- Autosomal recessive cerebellar ataxia - blindness - deafness
- Autosomal recessive cerebellar ataxia - psychomotor retardation
- Autosomal recessive cerebellar ataxia - saccadic intrusion
- Autosomal recessive cerebellar ataxia due to a DNA repair defect
- Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome
- Autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to TUD deficiency
- Autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome
- Autosomal recessive cerebelloparenchymal disorder type 3
- Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency
- Autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency
- Autosomal recessive disease associated with punctate palmoplantar keratoderma as a major feature
- Autosomal recessive disease with diffuse palmoplantar keratoderma as a major feature
- Autosomal recessive disease with focal palmoplantar keratoderma as a major feature
- Autosomal recessive dopa-responsive dystonia
- Autosomal recessive early-onset inflammatory bowel disease
- Autosomal recessive facio-digito-genital syndrome
- Autosomal recessive hyper-IgE syndrome
- Autosomal recessive hyper-IgE syndrome due to TYK2 deficiency
- Autosomal recessive infantile hypercalcemia
