Mondo Disease Ontology
5908 terms(s) returned
| Term Type: | Record: 5801 to 5850 of 5908 Records | Page: 117 of 119, First Previous Next Last | Show Records Per Page |
- autosomal recessive pericentral pigmentary retinopathy
- autosomal recessive polycystic kidney disease
- autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity
- autosomal recessive primary microcephaly
- autosomal recessive progressive external ophthalmoplegia
- autosomal recessive proximal renal tubular acidosis
- autosomal recessive secondary polycythemia not associated with VHL gene
- autosomal recessive severe congenital neutropenia
- autosomal recessive severe congenital neutropenia due to CSF3R deficiency
- autosomal recessive severe congenital neutropenia due to CXCR2 deficiency
- autosomal recessive severe congenital neutropenia due to G6PC3 deficiency
- autosomal recessive severe congenital neutropenia due to JAGN1 deficiency
- autosomal recessive sideroblastic anemia
- autosomal recessive spastic ataxia
- autosomal recessive spastic paraplegia type 59
- autosomal recessive spastic paraplegia type 60
- autosomal recessive spastic paraplegia type 66
- autosomal recessive spastic paraplegia type 67
- autosomal recessive spastic paraplegia type 68
- autosomal recessive spastic paraplegia type 69
- autosomal recessive spastic paraplegia type 70
- autosomal recessive spastic paraplegia type 71
- autosomal recessive spastic paraplegia type 76
- autosomal recessive spastic paraplegia type 78
- autosomal recessive spinocerebellar ataxia 10
- autosomal recessive spinocerebellar ataxia 11
- autosomal recessive spinocerebellar ataxia 12
- autosomal recessive spinocerebellar ataxia 13
- autosomal recessive spinocerebellar ataxia 14
- autosomal recessive spinocerebellar ataxia 15
- autosomal recessive spinocerebellar ataxia 16
- autosomal recessive spinocerebellar ataxia 17
- autosomal recessive spinocerebellar ataxia 18
- autosomal recessive spinocerebellar ataxia 2
- autosomal recessive spinocerebellar ataxia 20
- autosomal recessive spinocerebellar ataxia 7
- autosomal recessive spondylocostal dysostosis
- autosomal recessive spondylometaphyseal dysplasia, Megarbane type
- autosomal recessive syndromic cerebellar ataxia
- autosomal recessive syndromic intellectual disability
- autosomal recessive titinopathy
- autosomal semi-dominant severe lipodystrophic laminopathy
- autosomal systemic lupus erythematosus type 16
- autosome
- autotopagnosia
- avascular necrosis
- avascular necrosis of femoral head, primary, 1
- avascular necrosis of femoral head, primary, 2
- avian influenza
- avian leukosis
