A–Z DIRECTORY
Conditions beginning with I
- Ichthyosis with confettiAutosomal dominant
- Idiopathic infantile hypercalcemiaAutosomal recessive
- Idiopathic inflammatory myopathyPattern unknown
- Idiopathic pulmonary fibrosisAutosomal dominant
- IMAGe syndromeAutosomal dominant
- Imerslund-Gräsbeck syndromeAutosomal recessive
- Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndromeX-linked recessive
- Immune thrombocytopeniaPattern unknown
- Inclusion body myopathy with early-onset Paget disease and frontotemporal dementiaAutosomal dominant
- Incontinentia pigmentiX-linked dominant
- Infantile neuroaxonal dystrophyAutosomal recessive
- Infantile-onset ascending hereditary spastic paralysisAutosomal recessive
- Infantile-onset spinocerebellar ataxiaAutosomal recessive
- Inherited thyroxine-binding globulin deficiencyX-linked
- Intervertebral disc diseasePattern unknown
- Intestinal pseudo-obstructionAutosomal recessive · Autosomal dominant · X-linked
- Intrahepatic cholestasis of pregnancyAutosomal dominant
- Intranuclear rod myopathyNot inherited · Autosomal dominant
- IRAK-4 deficiencyAutosomal recessive
- Iron-refractory iron deficiency anemiaAutosomal recessive
- Isobutyryl-CoA dehydrogenase deficiencyAutosomal recessive
- Isolated congenital aspleniaAutosomal dominant · Pattern unknown
- Isolated Duane retraction syndromeAutosomal dominant · Autosomal recessive
- Isolated ectopia lentisAutosomal recessive · Autosomal dominant, inherited or a new variant
- Isolated growth hormone deficiencyAutosomal dominant · Autosomal recessive · X-linked recessive
- Isolated hyperchlorhidrosisAutosomal recessive
- Isolated hyperCKemiaAutosomal dominant
- Isolated lissencephaly sequenceX-linked dominant · Autosomal dominant
- Isolated Pierre Robin sequenceAutosomal dominant
- Isolated sulfite oxidase deficiencyAutosomal recessive
- Isovaleric acidemiaAutosomal recessive
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