|
Neuroleptic Resistant Schizophrenia |
Chain1150 |
This is a rare disease. |
|
Neuronal Ceroid Lipofuscinoses 6 |
Chain1151 |
This is a rare disease. |
|
Neuronal Ceroid Lipofuscinosis |
Chain1152 |
This is a rare disease. |
|
Neuronal ceroid lipofuscinosis, late infantile |
Chain1153 |
This is a rare disease. |
|
Neuropathy, Distal Hereditary Motor, Type IIB |
Chain1154 |
This is a rare disease. |
|
Axonal Charcot-Marie-Tooth Disease, Type 2F |
Chain1155 |
This is a rare disease. |
|
Neuropathy, Hereditary Sensory and Autonomic, Type V |
Chain1156 |
This is a rare disease. |
|
Loss of Pain & Temperature Perception |
Chain1157 |
This is a rare disease. |
|
Neuropathy, Hereditary Sensory, Type I |
Chain1158 |
This is a rare disease. |
|
Neuropathy, Hereditary Sensory, Type II |
Chain1159 |
This is a rare disease. |
|
Neurosensory deafness |
Chain1160 |
This is a rare disease. |
|
Neutropenia, Cyclic |
Chain1161 |
This is a rare disease. |
|
Neutropenia, Nonimmune Chronic Idiopathic, of Adults |
Chain1162 |
This is a rare disease. |
|
Neutropenia, Severe Congenital |
Chain1163 |
This is a rare disease. |
|
Neutropenia, Severe Congenital, Autosomal Recessive 3 |
Chain1164 |
This is a rare disease. |
|
Increased risk of suicidal thoughts and suicide when starting antidepressants |
Chain1165 |
New or worsening suicidalideation during Short-term Treatment with Antidepressants (Treatment-Emergent Suicidality) |
|
Niemann-Pick Disease |
Chain1166 |
This is a rare disease. |
|
Niemann-Pick Disease, Type A |
Chain1167 |
This is a rare disease. |
|
Niemann-Pick Disease, Type B |
Chain1168 |
This is a rare disease. |
|
Niemann-Pick Disease, Type C1 |
Chain1169 |
This is a rare disease. |
|
Niemann-Pick Disease, Type C2 |
Chain1170 |
This is a rare disease. |
|
Night Blindness, Congenital Stationary, Type 1 |
Chain1171 |
This is a rare disease. |
|
Night Blindness, Congenital Stationary, Type 1B |
Chain1172 |
This is a rare disease. |
|
Night Blindness, Congenital Stationary, Type 2 |
Chain1173 |
This is a rare disease. |
|
Night Blindness, Congenital Stationary, Type 2, Severe |
Chain1174 |
This is a rare disease. |
|
Night Blindness, Congenital Stationary, Type 2B |
Chain1175 |
This is a rare disease. |
|
Nightblindness, Congenital Stationary |
Chain1176 |
This is a rare disease. |
|
Nijmegen Breakage Syndrome |
Chain1177 |
This is a rare disease. |
|
Nocturnal Frontal Lobe Epilepsy, Type 4, with Nocturnal Wandering and Ictal Fear |
Chain1178 |
This is a rare disease. |
|
Non-classic Congenital Adrenal Hyperplasia |
Chain1179 |
This is a rare disease. |
|
Non-heterotaxy Cardiac Malformation |
Chain1180 |
This is a rare disease. |
|
Nonsmall Cell Lung Cancer, Bronchoalveolar Subtype, Resistant to Tyrosine Kinase Inhibitors |
Chain1181 |
This is a rare disease. |
|
Nonspecific Cardiac Conduction Defect |
Chain1182 |
This is a rare disease. |
|
Nonsyndromic Hearing Impairment |
Chain1183 |
This is a rare disease. |
|
Nonsyndromic Sensorineural Deafness |
Chain1184 |
This is a rare disease. |