Human Disease Ontology
19719 terms(s) returned
| Term Type: | Record: 4051 to 4100 of 19719 Records | Page: 82 of 395, First Previous Next Last | Show Records Per Page |
- allosomal inheritance
- alopecia
- alopecia areata
- alopecia universalis
- alopecia, neurologic defects, and endocrinopathy syndrome
- alopecia-mental retardation syndrome
- alopecia-mental retardation syndrome 1
- alopecia-mental retardation syndrome 2
- alopecia-mental retardation syndrome 3
- alopecia-mental retardation syndrome 4
- alpha 1-antitrypsin deficiency
- alpha chain disease
- alpha thalassemia
- alpha thalassemia-X-linked intellectual disability syndrome
- alpha thalassemia-intellectual disability syndrome type 1
- alpha,beta-unsaturated monocarboxylic acid
- alpha-2-plasmin inhibitor deficiency
- alpha-amino acid
- alpha-gal syndrome
- alpha-mannosidosis
- alpha-methylacyl-CoA racemase deficiency
- alpha-thalassemia myelodysplasia syndrome
- alteration of appetite
- alteration of consciousness
- altered mental status
- altered_gene_product_level
- altered_gene_product_sequence
- alternating esotropia
- alternating exotropia
- alternating hemiplegia of childhood
- alveolar echinococcosis
- alveolar periostitis
- alveolar rhabdomyosarcoma
- alveolar soft part sarcoma
- alveoli adenoma
- alveolus
- alveolus of lung
- amaurosis
- amaurosis fugax
- amblyopia
- amebiasis
- amelanotic melanoma
- ameloblastoma
- amelogenesis imperfecta
- amelogenesis imperfecta hypomaturation type 2A2
- amelogenesis imperfecta hypomaturation type 2A3
- amelogenesis imperfecta hypomaturation type 2A4
- amelogenesis imperfecta hypomaturation type 2A5
- amelogenesis imperfecta type 1A
- amelogenesis imperfecta type 1B
