Mondo Disease Ontology
4789 terms(s) returned
| Term Type: | Record: 2201 to 2250 of 4789 Records | Page: 45 of 96, First Previous Next Last | Show Records Per Page |
- set of lower jaw teeth
- set of muscles of vertebral column
- set of upper jaw teeth
- setariasis
- setting-Sun phenomenon, familial benign
- severe Canavan disease
- severe X-linked mitochondrial encephalomyopathy
- severe achondroplasia-developmental delay-acanthosis nigricans syndrome
- severe acute respiratory syndrome
- severe autoimmune neutropenia
- severe chronic neutropenia
- severe combined immunodeficiency
- severe combined immunodeficiency disease, IL2RG and, RAG1-related, crab-eating macaque
- severe combined immunodeficiency disease, PRKDC-related, dog
- severe combined immunodeficiency disease, PRKDC-related, horse
- severe combined immunodeficiency disease, RAG1-related, dog
- severe combined immunodeficiency disease, non-human animal
- severe combined immunodeficiency disease, pig
- severe combined immunodeficiency due to CARD11 deficiency
- severe combined immunodeficiency due to CARMIL2 deficiency
- severe combined immunodeficiency due to CD70 deficiency
- severe combined immunodeficiency due to CORO1A deficiency
- severe combined immunodeficiency due to DCLRE1C deficiency
- severe combined immunodeficiency due to DNA-PKcs deficiency
- severe combined immunodeficiency due to IKK2 deficiency
- severe combined immunodeficiency due to LAT deficiency
- severe combined immunodeficiency due to LCK deficiency
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency
- severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive
- severe congenital hypochromic anemia with ringed sideroblasts
- severe congenital myelofibrosis-pancytopenia-intellectual disability-neurologic and ophthalmic abnormalities syndrome
- severe congenital nemaline myopathy
- severe congenital neutropenia
- severe cutaneous adverse reaction
- severe dermatitis-multiple allergies-metabolic wasting syndrome
- severe early-childhood-onset retinal dystrophy
- severe early-onset axonal neuropathy due to MFN2 deficiency
- severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency
- severe early-onset pulmonary alveolar proteinosis due to MARS deficiency
- severe equine asthma
- severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome
- severe hemophilia A
- severe hemophilia B
- severe hypophosphatasia
- severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome
- severe ichthyosis vulgaris
- severe idiopathic neutropenia
- severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome
- severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia
- severe intellectual disability-hypotonia-strabismus-coarse face-planovalgus syndrome
