Phenotypes for disease #00842 (GAND;MRD18 (GAND syndrome (GAND, MRD18)), OMIM:615074)

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AscendingPhenotype ID     

Phenotype details     

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Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

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Birth_Details     

Protein     

Owner     

Individual ID     
0000060534 Mental retardation, autosomal dominant 18 (OMIM:615074) - - Isolated (sporadic) - - - - - - Daniel Trujillano 00080965
0000186538 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) HP:0002342 Intellectual disability, moderate GAND Isolated (sporadic) - 14y - - - - Emanuela Leonardi 00246694
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