Wikidata

(Q1915681)

English

Meckel syndrome

a rare, lethal, ciliopathic, genetic disorder with malformations of the urinary system, of central nervous system, hepatic developmental defects, and pulmonary hypoplasia.

  • Meckel-Gruber syndrome
  • Meckel–Gruber Syndrome
  • Gruber Syndrome
  • Dysencephalia Splanchnocystica
  • Meckel's syndrome
In more languages

Statements

instance of
rare disease
0 references
class of disease
0 references
NCI Thesaurus ID
C98978
0 references
Commons category
Meckel syndrome
0 references

Identifiers

KEGG ID
H00261
0 references
ICD-11 ID (MMS)
LD2F.13
subject named as
Meckel-Gruber syndrome
0 references
YSO ID
19890
subject named as
Meckelin oireyhtymä
Meckels syndrom
Meckel's syndrome
1 reference
stated in
YSO-Wikidata mapping project
retrieved
7 February 2022
 
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