Mondo Disease Ontology
931 terms(s) returned
Term Type: | Record: 1 to 50 of 931 Records | Page: 1 of 19, First Previous Next Last | Show Records Per Page |
- N syndrome
- N-acetylaspartate deficiency
- N1 diffuse large B-cell lymphoma
- NAA10-related syndrome
- NACC1-related neurodevelopmental disorder with epilepsy, cataracts and episodic irritability
- NAD(P)HX dehydratase deficiency
- NAFLD1
- NARP syndrome
- NDE1-related microhydranencephaly
- NEK9-related lethal skeletal dysplasia
- NIK deficiency
- NK cell deficiency
- NK-cell enteropathy
- NKX2-1 related choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction
- NKX2.5-related congenital, conduction and myopathic heart disease
- NMNAT1-related retinopathy
- NOG-related symphalangism spectrum disorder
- NPHP3-related Meckel-like syndrome
- NR2F2 related multiple congenital anomalies/dysmorphic syndrome
- NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance
- NTHL1-deficiency tumor predisposition syndrome
- NTRK fusion positive cancer
- NYX-related retinopathy
- Naegeli-Franceschetti-Jadassohn syndrome
- Nager acrofacial dysostosis
- Nairobi sheep disease
- Nance-Horan syndrome
- Nathalie syndrome
- Naxos disease
- Nelson syndrome
- Nematoda infectious disease
- Neorickettsia infectious disease
- Nestor-Guillermo progeria syndrome
- Netherton syndrome
- Neu-Laxova syndrome
- Neu-Laxova syndrome 1
- Neu-Laxova syndrome 2
- Neuhauser anomaly
- Nevada syndrome
- Newcastle disease
- Newfoundland cone-rod dystrophy
- Nezelof syndrome
- Nguyen syndrome
- Nidovirales infectious disease
- Niemann-Pick disease
- Niemann-Pick disease type A
- Niemann-Pick disease type B
- Niemann-Pick disease type C
- Niemann-Pick disease type C, adult neurologic onset
- Niemann-Pick disease type C, juvenile neurologic onset