Mondo Disease Ontology
2318 terms(s) returned
| Term Type: Class | Record: 1901 to 1950 of 2318 Records | Page: 39 of 47, First Previous Next Last | Show Records Per Page |
- neuropathy, hereditary sensory, type 1D
- neuropathy, hereditary sensory, type 1F
- neuropathy, hereditary sensory, type 2C
- neuropathy, painful
- neuropathy, small fiber
- neuropathy, with paraprotein in serum, cerebrospinal fluid and urine
- neuroretinitis
- neurosarcoidosis
- neuroschistosomiasis
- neurosyphilis
- neurothekeoma
- neurotic depression
- neurotic disorder
- neurotic excoriation
- neurotoxin
- neurotransmitter
- neurotransmitter agent
- neurotransmitter agent therapy
- neurotransmitter receptor activity
- neurotransmitter receptor activity involved in regulation of postsynaptic membrane potential
- neurotransmitter receptor regulator activity
- neurotransmitter secretion
- neurotransmitter secretion involved in regulation of skeletal muscle contraction
- neurotransmitter transport
- neurotrophic keratoconjunctivitis
- neurotrophic keratopathy
- neurovascular disorder
- neurula embryo
- neurula stage
- neutral amino acid transport
- neutral glycosphingolipid
- neutral lipid storage disease
- neutral lipid storage myopathy
- neutropenia
- neutropenia, chronic familial
- neutropenia, lethal congenital, with eosinophilia
- neutropenia, severe congenital, 1, autosomal dominant
- neutropenia, severe congenital, 10, autosomal recessive
- neutropenia, severe congenital, 11, autosomal dominant
- neutropenia, severe congenital, 2, autosomal dominant
- neutropenia, severe congenital, 8, autosomal dominant
- neutropenia, severe congenital, 9, autosomal dominant
- neutropenia-monocytopenia-deafness syndrome
- neutrophil
- neutrophil actin dysfunction
- neutrophil chemotaxis
- neutrophil immunodeficiency syndrome
- neutrophil migration
- neutrophillic
- neutrophillic cytoplasm
