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Ontology Browser

Term:
X-Linked Mental Retardation with Isolated Growth Hormone Deficiency (DOID:9004048)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
adrenoleukodystrophy +   
Alazami Syndrome  
Aldred Syndrome 
Allan-Herndon-Dudley syndrome  
alpha thalassemia-X-linked intellectual disability syndrome  
Arena Syndrome 
Atkin Syndrome  
CATARACTS, GROWTH HORMONE DEFICIENCY, SENSORY NEUROPATHY, SENSORINEURAL HEARING LOSS, AND SKELETAL DYSPLASIA  
Charcot-Marie-Tooth disease X-linked recessive 4  
Chromosome Xp11.3 Deletion Syndrome  
CK syndrome  
Classical Lissencephalies and Subcortical Band Heterotopias +   
Coffin-Lowry syndrome  
Combined Pituitary Hormone Deficiency, 2  
Combined Pituitary Hormone Deficiency, 3  
Combined Pituitary Hormone Deficiency, 4  
creatine transporter deficiency  
Danon disease  
Encephalopathy with Intracranial Calcification, Growth Hormone Deficiency, Microcephaly, and Retinal Degeneration 
Faciogenital Dysplasia with Attention Deficit-Hyperactivity Disorder 
FG syndrome +   
fragile X syndrome +   
Idiopathic Short Stature, Autosomal  
isolated growth hormone deficiency type IA  
isolated growth hormone deficiency type IB  
isolated growth hormone deficiency type II  
isolated growth hormone deficiency type III  
Isolated Growth Hormone Deficiency Type V  
Isolated Growth Hormone Deficiency, Partial  
Kowarski Syndrome  
Lesch-Nyhan syndrome +   
Menkes disease +   
Mental Retardation X-Linked, South African Type 
Mental Retardation, X-Linked 102  
Mental Retardation, X-Linked 95  
Mental Retardation, X-Linked, Syp-Related 
methylmalonic acidemia and homocysteinemia cblX type  
mucopolysaccharidosis II  
non-syndromic X-linked intellectual disability +   
Pituitary Dwarfism with Large Sella Turcica 
Plagiocephaly and X-Linked Mental Retardation 
Ppm-X Syndrome 
pyruvate decarboxylase deficiency +   
Rett syndrome +   
Roifman Syndrome  
severe congenital encephalopathy due to MECP2 mutation  
syndromic microphthalmia 1  
syndromic X-linked intellectual disability +   
Tranebjaerg Svejgaard syndrome 
Wittwer Syndrome  
X-linked intellectual disability-psychosis-macroorchidism syndrome  
X-Linked Mental Retardation Gustavson Type 
X-linked mental retardation with cerebellar hypoplasia and distinctive facial appearance  
X-Linked Mental Retardation with Isolated Growth Hormone Deficiency  
X-Linked Mental Retardation with Panhypopituitarism  

Synonyms
Exact Synonyms: X-linked mental retardation with growth hormone deficiency
Primary IDs: MESH:C564712

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