Term info
definition
An characteristic of a disease in which the disease is manifested as an isolated feature.
id
MONDO:0021128
Term relations
Related from:
has characteristic
- non-syndromic polydactyly
- polycystic liver disease 1
- orofacial cleft 12
- isolated osteopoikilosis
- non-syndromic urogenital tract malformation
- Fiedler's myocarditis
- orofacial cleft 10
- orofacial cleft 13
- isolated focal palmoplantar keratoderma
- isolated diffuse palmoplantar keratoderma
- non-syndromic respiratory or mediastinal malformation
- non-syndromic intestinal malformation
- non-syndromic developmental defect of the eye
- non-syndromic central nervous system malformation
- non-syndromic esophageal malformation
- non-syndromic gastroduodenal malformation
- isolated craniosynostosis
- isolated dystonia
- genetic non-syndromic obesity
- isolated cleft palate
- orofacial cleft 1
- orofacial cleft 11
- inherited isolated nail anomaly
- nonsyndromic genetic hearing loss
- isolated congenital ectropion
- Laubry-Pezzi syndrome
- isolated optic neuritis
- isolated congenital alacrima
- non-syndromic male infertility due to sperm motility disorder
- inherited non-syndromic ichthyosis
- non-syndromic intellectual disability
- orofacial cleft 9
- isolated microphthalmia
- orofacial cleft 4
- orofacial cleft 15
- isolated cleft lip
- familial isolated arrhythmogenic right ventricular dysplasia
- isolated anorectal malformation
- isolated agammaglobulinemia
- isolated Klippel-Feil syndrome
- isolated punctate palmoplantar keratoderma
- congenital isolated adrenocorticotropic hormone deficiency
- isolated glycerol kinase deficiency