Disorders
0-9 | A-B | C-D | E-F | G-H | I-J | K-L | M-N | O-P | Q-R | S-T | U-V | W-X | Y-Z
- Ichthyosis Bullosa of Siemens OMIM
- Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome OMIM
- Ichthyosis Prematurity Syndrome OMIM
- Ichthyosis Vulgaris OMIM
- Ichthyosis, Hystrix-like, with Deafness OMIM
- Ichthyosis, Leukocyte Vacuoles, Alopecia, and Sclerosing Cholangitis OMIM
- Ichthyosis, X-Linked OMIM
- IMAGe Syndrome OMIM
- Iminoglycinuria OMIM
- Immunodeficiency due to Defect in CD3-Gamma OMIM
- Immunodeficiency with Hyper-IgM, Type 2 OMIM
- Immunodeficiency with Hyper-IgM, Type 3 OMIM
- Immunodeficiency with Hyper-IgM, Type 5 OMIM
- Immunodeficiency without Anhidrotic Ectodermal Dysplasia OMIM
- Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia OMIM
- Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome OMIM
- Inclusion Body Myopathy 3 OMIM
- Inclusion Body Myopathy with Paget Disease of Bone and/or Frontotemporal Dementia GeneReviewOMIM
- Incontinentia Pigmenti GeneReviewOMIM
- Infantile-Onset Spinocerebellar Ataxia GeneReviewOMIM
- Infection-induced Acute Encephalopathy 3, Susceptibility to OMIM
- Inflammatory Bowel Disease 25, Autosomal Recessive OMIM
- Inflammatory Bowel Disease 28, Autosomal Recessive OMIM
- Insulin-Like Growth Factor I Deficiency OMIM
- Insulin-Like Growth Factor I, Resistance to OMIM
- Intellectual Disability Multi-Gene Panels
- Interleukin 1 Receptor Antagonist Deficiency OMIM
- Interleukin 2 Receptor Alpha Chain Deficiency OMIM
- Intermediate Charcot-Marie-Tooth Neuropathy OMIM
- DNM2-Related Intermediate Charcot-Marie-Tooth Neuropathy GeneReviewOMIM
- GDAP1-Related Intermediate Charcot-Marie-Tooth Neuropathy OMIM
- KARS-Related Intermediate Charcot-Marie-Tooth Neuropathy OMIM
- MPZ-Related Intermediate Charcot-Marie-Tooth Neuropathy OMIM
- YARS-Related Intermediate Charcot-Marie-Tooth Neuropathy OMIM
- Intrinsic Factor Deficiency OMIM
- IPEX Syndrome GeneReviewOMIM
- IRAK4 Deficiency OMIM
- IRF6-Related Disorders GeneReviewOMIM
- Popliteal Pterygium Syndrome OMIM
- van der Woude Syndrome OMIM
- Iridogoniodysgenesis, Type 1 OMIM
- Iris Hypoplasia OMIM
- Iron Overload, Autosomal Dominant OMIM
- Iron-Refractory Iron Deficiency Anemia OMIM
- Isobutyryl-CoA Dehydrogenase Deficiency OMIM
- Isolated Congenital Digital Clubbing OMIM
- Isolated Follicle-Stimulating Hormone Deficiency OMIM
- Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency GeneReviewOMIM
- CHD7-Related Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency OMIM
- FGF8-Related Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency OMIM
- FGFR1-Related Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency OMIM
- GNRH1-Related Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency OMIM
- GNRHR-Related Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency OMIM
- KAL1-Related Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency OMIM
- KISS1-Related Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency OMIM
- KISS1R-Related Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency OMIM
- PROK2-Related Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency OMIM
- PROKR2-Related Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency OMIM
- TACR3-Related Isolated Gonadotropin-Releasing Hormone (GnRH) Deficiency OMIM
- Isolated Growth Hormone Deficiency, Type IA OMIM
- Isolated Growth Hormone Deficiency, Type IB, GH1-Related OMIM
- Isolated Growth Hormone Deficiency, Type IB, GHRHR-Related OMIM
- Isolated Growth Hormone Deficiency, Type II OMIM
- Isolated Growth Hormone Deficiency, Type III OMIM
- Isolated Microphthalmia 5 OMIM
- Isolated Nonsyndromic Congenital Heart Disease/Defects OMIM
- Isolated Persistent Hypermethioninemia OMIM
- Isovaleric Acidemia OMIM
- Jacobsen Syndrome OMIM
- JAK2-Related Budd-Chiari Syndrome OMIM
- Jalili Syndrome OMIM
- Jawad Syndrome OMIM
- Jervell and Lange-Nielsen Syndrome GeneReviewOMIM
- Long QT Syndrome 1 OMIM
- Long QT Syndrome 5 OMIM
- Joubert Syndrome and Related Disorders GeneReviewOMIM
- AHI1-Related Joubert Syndrome OMIM
- ARL13B-Related Joubert Syndrome OMIM
- C5orf42-Related Joubert Syndrome OMIM
- CC2D2A-Related Joubert Syndrome OMIM
- CEP290-Related Joubert Syndrome OMIM
- CEP41-Related Joubert Syndrome OMIM
- INPP5E-Related Joubert Syndrome OMIM
- KIF7-Related Joubert Syndrome OMIM
- NPHP1-Related Joubert Syndrome OMIM
- OFD1-Related Joubert Syndrome OMIM
- RPGRIP1L-Related Joubert Syndrome OMIM
- TCTN1-Related Joubert Syndrome OMIM
- TCTN2-Related Joubert Syndrome OMIM
- TCTN3-Related Joubert Syndrome OMIM
- TMEM138-Related Joubert Syndrome OMIM
- TMEM216-Related Joubert Syndrome OMIM
- TMEM231-Related Joubert Syndrome OMIM
- TMEM237-Related Joubert Syndrome OMIM
- TMEM67-Related Joubert Syndrome OMIM
- TTC21B-Related Joubert Syndrome OMIM
- Joubert Syndrome and Related Disorders Multi-Gene Panels
- Junctional Epidermolysis Bullosa GeneReviewOMIM
- COL17A1-Related Junctional Epidermolysis Bullosa OMIM
- LAMA3-Related Junctional Epidermolysis Bullosa OMIM
- LAMB3-Related Junctional Epidermolysis Bullosa OMIM
- LAMC2-Related Junctional Epidermolysis Bullosa OMIM
- Juvenile Hereditary Hemochromatosis GeneReviewOMIM
- HAMP-Related Juvenile Hemochromatosis OMIM
- HJV (HFE2)-Related Juvenile Hemochromatosis OMIM
- Juvenile Myoclonic Epilepsy OMIM
- CACNB4-Related Juvenile Myoclonic Epilepsy OMIM
- CLCN2-Related Juvenile Myoclonic Epilepsy OMIM
- EFHC1-Related Juvenile Myoclonic Epilepsy OMIM
- EJM2-Related Juvenile Myoclonic Epilepsy OMIM
- EJM3-Related Juvenile Myoclonic Epilepsy OMIM
- EJM4-Related Juvenile Myoclonic Epilepsy OMIM
- GABRA1-Related Juvenile Myoclonic Epilepsy OMIM
- GABRD-Related Juvenile Myoclonic Epilepsy OMIM
- Juvenile Polyposis Syndrome GeneReviewOMIM
- BMPR1A-Related Juvenile Polyposis OMIM
- SMAD4-Related Juvenile Polyposis OMIM
- Juvenile Polyposis/Hereditary Hemorrhagic Telangiectasia Syndrome OMIM