Disease Index
9,486 diseasesneonatal myasthenia gravis
Human disease
MeSH: D020941
neonatal osteosclerotic dysplasia
human disease
neonatal scleroderma
human disease
neonatal severe cardiopulmonary failure due to mitochondrial methylation defect
human disease
neonatal severe primary hyperparathyroidism
3.5 mM) from birth and associated with major hyperparathyroidism.
MeSH: C563375
neoplasm of the nailbed
neoplasm involving a nail
neovascular glaucoma
Human disease
MeSH: D015355
nephrogenic diabetes insipidus
impaired renal function disease characterized by a complete or partial resistance of the kidneys to arginine vasopressin (AVP)
ICD: N25.1MeSH: D018500
nephrogenic diabetes insipidus-intracranial calcification syndrome
This syndrome is characterised by nephrogenic diabetes insipidus, intracerebral calcifications, intellectual deficit, short stature and facial dysmorphism
ICD: N25.1MeSH: C535949
nephrogenic syndrome of inappropriate antidiuresis
ICD: E22.2MeSH: C564491
nephrogenic systemic fibrosis
medical condition
MeSH: D054989
nephronophthisis
congenital disorder of urinary system
nephronophthisis 16
nephronophthisis that has material basis in homozygous mutation in the ANKS6 gene on chromosome 9q22
nephropathic infantile cystinosis
nephropathy secondary to a storage or other metabolic disease
human disease
nephropathy-deafness-hyperparathyroidism syndrome
MeSH: C536401
nephrosis-deafness-urinary tract-digital malformations syndrome
MeSH: C536402
nephrotic syndrome type 1
familial nephrotic syndrome characterized by prenatal onset of massive proteinuria followed by steroid resistant renal disease that has material basis in homozygous or compound heterozygous mutation in the NPHS1 gene on chromosome 19q13
MeSH: C535761
nephrotic syndrome type 7
human disease
nephrotic syndrome-deafness-pretibial epidermolysis bullosa syndrome
human disease
MeSH: C563798
nervous system anomaly with eye involvement
human disease
nervous system heredodegenerative disease
human disease
MeSH: D020271
nervous system malformations
congenital conditions that stem from damage to, or abnormal development of, the budding nervous system
ICD: Q00-Q07MeSH: D009421
Nestor-Guillermo progeria syndrome
human disease
Netherton syndrome
Human disease
ICD: Q80.8MeSH: D056770
Neu-Laxova syndrome
medical condition
MeSH: C536405
Neuhauser anomaly
human disease
ICD: Q25.4
neural tube defect
congenital disorder of the nervous system
ICD: Q00MeSH: D009436
neurenteric cyst
human disease
neuro-ophthalmological disease
human disease