Mondo Disease Ontology
5621 terms(s) returned
| Term Type: | Record: 1051 to 1100 of 5621 Records | Page: 22 of 113, First Previous Next Last | Show Records Per Page |
- obsolete aspergillosis
- obsolete aspirin allergy
- obsolete astroblastoma
- obsolete astrocytoma
- obsolete asymptomatic COVID-19 infection
- obsolete ataxia syndrome
- obsolete ataxia with dementia
- obsolete ataxia with oculomotor apraxia type 2
- obsolete ataxia-oculomotor apraxia
- obsolete ataxia-telangiectasia-like disorder
- obsolete athyreotic congenital hypothyroidism
- obsolete atrial appendage anomaly
- obsolete atrial defect and interatrial communication
- obsolete atrial septal defect coronary sinus
- obsolete atrial standstill
- obsolete atrioventricular septal defect 3
- obsolete atrioventricular valve anomaly
- obsolete atrophic vulva
- obsolete atrophy of lacrimal gland
- obsolete atrophy of prostate
- obsolete atypical Mycobacteriosis, familial
- obsolete atypical chronic myeloid leukemia
- obsolete atypical lipomatous tumor
- obsolete atypical papilloma of choroid plexus
- obsolete atypical teratoid rhabdoid tumor
- obsolete australia antigen
- obsolete autism
- obsolete autism susceptibility 1
- obsolete autoimmune disease
- obsolete autoimmune disease of skin and connective tissue
- obsolete autoimmune disease with skin involvement
- obsolete autoimmune disorder of urogenital tract
- obsolete autoimmune enteropathy type 2
- obsolete autoimmune hemolytic anemia
- obsolete autoimmune lymphoproliferative syndrome type 3
- obsolete autoimmune neurological channelopathy
- obsolete autoimmune pancreatitis type 1
- obsolete autoimmune polyendocrine syndrome type 2
- obsolete autoimmune polyendocrinopathy syndrome
- obsolete autoinflammatory syndrome with immune deficiency
- obsolete autoinflammatory syndrome with skin involvement
- obsolete autonomic peripheral neuropathy
- obsolete autosomal dominant Charcot-Marie-Tooth disease type 2G
- obsolete autosomal dominant Opitz G/BBB syndrome
- obsolete autosomal dominant cerebellar ataxia
- obsolete autosomal dominant diffuse mutilating palmoplantar keratoderma
- obsolete autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature
- obsolete autosomal dominant disease with diffuse palmoplantar keratoderma as a major feature
- obsolete autosomal dominant hereditary axonal motor and sensory neuropathy
- obsolete autosomal dominant hereditary demyelinating motor and sensory neuropathy
