back 1
2
3
5
A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
R
S
T
U
V
W
X
Y
Z
List of all diseases starting with N
- N-ACETYLASPARTYLGLUTAMATE ACCUMULATION MIM=
- N-ACETYLGLUTAMATE SYNTHETASE DEFICIENCY; NAGS DEFICIENCY MIM=237310
- NARP SYNDROME MIM=551500
- NEONATAL DIABETES MELLITUS, ENTEROPATHY, THROMBOCYTOPENIA AND ENDOCRINOPATHY (IPEX) MIM=304790
- NEPHROTIC SYNDROME, TYPE 14 (NPHS14) MIM=617575
- NEPHROTIC SYNDROME, TYPE 7 (NPHS7) MIM=615008
- NEU-LAXOVA SYNDROME 1; NLS1 (PHGDH) MIM=256520
- NEU-LAXOVA SYNDROME 2; NLS2 (PSAT) MIM=616038
- NEUROBLASTOMA, SUSCEPTIBILITY TO MIM=256700
- NEURODEGENERATION WITH ATAXIA, DYSTONIA, AND GAZE PALSY, CHILDHOOD-ONSET; NADGP (SQSTM1) MIM=617145
- NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 1; NBIA1 (PKAN) MIM=234600
- NEURODEGENERATION WITH BRAIN IRON ACCUMULATION 5; NBIA5 (WDR45) MIM=300894
- NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS (NEDHAHM) MIM=6187
- NEURODEVELOPMENTAL DISORDER, MITOCHONDRIAL, WITH ABNORMAL MOVEMENTS AND LACTIC ACIDOSIS, WITH OR WITHOUT SEIZURES MIM=617710<
- NEUROLOGIC, ENDOCRINE, AND PANCREATIC DISEASE, MULTISYSTEM, INFANTILE-ONSET (IMNEPD) MIM=616263
- NEUROPATHY, HEREDITARY MOTOR AND SENSORY, RUSSE TYPE (HMSNR) MIM=605285
- NEUTRAL LIPID STORAGE DISEASE WITH MYOPATHY (NLSDM) MIM=610717
- NEWBORNS, PREMATURE INFANTS, TRANSIENT IMMATURITY OF TRANSPORT SYSTEMS OR ENZYMES MIM=
- NICOTINAMIDE ADENINE DINUCLEOTIDE DEFICIENCY MIM=---
- NIEMANN-PICK DISEASE TYPE A MIM=257200
- NIEMANN-PICK DISEASE TYPE B MIM=607616
- NIEMANN-PICK DISEASE TYPE C1 (NPC1) MIM=257220
- NIEMANN-PICK DISEASE, TYPE C2 (NPC2) MIM=607625
- NO METABOLIC DISEASE / ENDOCRINE DISORDER [DD] MIM=---
- NONALCOHOLIC FATTY LIVER DISEASE [DD] MIM=---
- NUCLEOTIDE DEPLETION SYNDROME MIM=
- NUTRITION:COFFFEE CONSUMPTION [EXTERNAL] MIM=