Homepage > Rare diseases > Search

Search for a rare disease

*
(*) mandatory field

Congenital lactase deficiency

Suggest an update
Your message has been sent Your message has not been sent. Please contact an administrator.
Disease definition

Congenital lactase deficiency is a rare severe gastrointestinal disorder in newborns primarily reported in Finland and characterized clinically by watery diarrhea on feeding with breast-milk or lactose-containing formula.

ORPHA:53690

Classification level: Disorder

Prevalence: -

Inheritance: Autosomal recessive

Age of onset:

ICD-10: E73.0

ICD-11: 5C61.61

OMIM: 223000

UMLS: C0268179

MeSH: C562600

MedDRA: 10086148

A summary on this disease is available in Español (2012) Deutsch (2012) Italiano (2012) Nederlands (2012) Ελληνικά (2012.pdf)
The documents contained in this website are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.