|
Joubert Syndrome 5 |
Chain894 |
This is a rare disease. |
|
Joubert syndrome 6 |
Chain895 |
This is a rare disease. |
|
Juvenile Absence Epilepsy |
Chain896 |
This is a rare disease. |
|
Adult Metachromatic Leukodystrophy |
Chain897 |
This is a rare disease. |
|
Arylsulfatase A, Allele I |
Chain898 |
This is a rare disease. |
|
Juvenile Metachromatic Leukodystrophy |
Chain899 |
This is a rare disease. |
|
Juvenile Myelomonocytic Leukemia |
Chain900 |
This is a rare disease. |
|
Juvenile Myoclonic Epilepsy |
Chain901 |
This is a rare disease. |
|
Juvenile Myoclonic Epilepsy, Type 1 |
Chain902 |
This is a rare disease. |
|
Juvenile Parkinson Disease 2 |
Chain903 |
This is a rare disease. |
|
Juvenile Polyposis/Hereditary Hemorrhagic Telangiectasia Syndrome |
Chain904 |
This is a rare disease. |
|
Kallmann Syndrome |
Chain905 |
This is a rare disease. |
|
Kallmann Syndrome 2 |
Chain906 |
This is a rare disease. |
|
Kartagener Syndrome |
Chain907 |
This is a rare disease. |
|
Keratitis-ichthyosis-deafness Syndrome |
Chain910 |
This is a rare disease. |
|
Left Ventricular Noncompaction, Isolated |
Chain933 |
This is a rare disease. |
|
Keratoderma, Palmoplantar, with Deafness Deafness, Nonsyndromic Sensorineural |
Chain912 |
This is a rare disease. |
|
Kidd blood group variant |
Chain913 |
This is a rare disease. |
|
Knuckle pads, Leukonychia, Sensorineural Deafness |
Chain914 |
This is a rare disease. |
|
Kowarski Syndrome |
Chain915 |
This is a rare disease. |
|
Larsen Syndrome, Autosomal Dominant |
Chain916 |
This is a rare disease. |
|
Late Fetal Loss |
Chain917 |
This is a rare disease. |
|
Late Infantile Metachromatic Leukodystrophy |
Chain918 |
This is a rare disease. |
|
Lateral Temporal Lobe Epilepsy |
Chain919 |
This is a rare disease. |
|
Leber Congenital Amaurosis 10 |
Chain920 |
This is a rare disease. |
|
Leber Congenital Amaurosis, Type I |
Chain921 |
This is a rare disease. |
|
Leber Congenital Amaurosis, Type III |
Chain922 |
This is a rare disease. |
|
Leber Congenital Amaurosis, Type VI |
Chain923 |
This is a rare disease. |
|
Leber Congenital Amaurosis, Type VII |
Chain924 |
This is a rare disease. |
|
Leber Hereditary Optic Neuropathy |
Chain925 |
This is a rare disease. |
|
Leber Hereditary Optic Neuropathy, Severe |
Chain926 |
This is a rare disease. |
|
Leber Optic Atrophy (Analysis A) |
Chain927 |
This is a rare disease. |
|
Leber Optic Atrophy (Analysis B) |
Chain928 |
This is a rare disease. |
|
Leber Hereditary Optic Neuropathy |
Chain929 |
This is a rare disease. |
|
Deafness, Aminogycloside-induced |
Chain930 |
This is a rare disease. |