Disease #00842 (GAND;MRD18 (GAND syndrome (GAND, MRD18)), OMIM:615074)

Official abbreviation GAND;MRD18
Name GAND syndrome (GAND, MRD18)
OMIM ID 615074
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene GATAD2B
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Genes screened

Variants in genes

Variants     

Panel size     

Owner     
00080965 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - GAND;MRD18 Mental retardation, autosomal dominant 18 (OMIM:615074) GATAD2B GATAD2B 1 1 Daniel Trujillano
00246694 P18 PubMed: Vera 2020 - F no Italy;(Italy) Italian - 1 - - GAND;MRD18 birth 41+2w; birth weight 4000g, length 54.5cm, OFC 37cm; weight +1.5 SD, height 2 SD, OFC +3.4 SD; no neonatal hypotonia; global developmental delay (HP:0001263); motor delay; 14m-sit; 22m-walk; speech delay (HP:0002463); 18m-first words; moderate intellectual deficiency; behavioral problems; no feeding difficulties; no sleep disorder; no constipation; no deafness; vision disorder; no strabismus; MRI brain abnormalities, white matter signal, myelination delay, ventriculomegaly enlarged CSF space; macrocephaly (HP:0000256); dysmorphic features; broad forehead; no narrow palpebral fissures; deeply set eyes (HP:0000490); hypertelorism; periorbital fullness; ear anomalies; no large/prominent nose; no tubular shaped nose; wide nasal base; no short philtrum; broad mouth (HP:0000154); no downturned mouth; thin upper lip; pointed chin; no blond hair; no thin hair; hands/feet anomalies; long fingers; no clinodactyly; ataxia (HP:0001251); dystonia (HP:0001332) - GATAD2B 1 1 Emanuela Leonardi
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.