Phenotypes for disease #04635 (NEDRIHF;MRD31 (neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties), OMIM:616158)

2 entries on 1 page. Showing entries 1 - 2.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000060467 Mental retardation, autosomal dominant 31 (OMIM:616158) - - Isolated (sporadic) - - - - - Daniel Trujillano 00080898
0000304726 Macrocephaly, Absent speech, Gait disturbance, Motor delay, Global developmental delay, Tall stature - - Isolated (sporadic) 11y - - - - Andreas Laner 00412735
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