Disease Browser
|
Parent Node: Eczema (D004485) | Parent Node: Foot Deformities, Congenital (D005532) | Parent Node: Growth Disorders (D006130) | Parent Node: Hand Deformities, Congenital (D006228) | Parent Node: Psychomotor Disorders (D011596) | ..Starting node ..Growth Retardation, Small and Puffy Hands and Feet, and Eczema (C565528)
| Child Nodes:
|
Sister Nodes: | ..Apraxias (D001072) 10
| ..Bowen-Conradi syndrome (C537081)
| ..C SYNDROME (OMIM:211750)
| ..CHROMOSOME 3pter-p25 DELETION SYNDROME (OMIM:613792)
| ..De Hauwere Leroy Adriaenssens syndrome (C535991)
| ..Developmental Delay, Epilepsy, and Neonatal Diabetes (C565253)
| ..Diaminopentanuria (C565630)
| ..Dystonia, Dopa-Responsive, due to Sepiapterin Reductase Deficiency (C562657)
| ..Edinburgh Malformation Syndrome (C563051)
| ..Fumaric aciduria (C538191)
| ..Genitopatellar Syndrome (C565255)
| ..Growth Retardation, Small and Puffy Hands and Feet, and Eczema (C565528)
| ..Hypomyelination, Global Cerebral (C567847)
| ..Ichthyosis prematurity syndrome (C536271)
| ..Kozlowski Rafinski Klicharska syndrome (C537509)
| ..MacDermot Winter syndrome (C537714)
| ..Megarbane syndrome (C536145)
| ..Myelodysplasia, Immunodeficiency, Facial Dysmorphism, Short Stature, and Psychomotor Delay (C563345)
| ..Phosphoglycerate Dehydrogenase Deficiency (C566618)
| ..Phosphoserine Aminotransferase Deficiency (C567032)
| ..Polyhydramnios, Megalencephaly, And Symptomatic Epilepsy (C567020)
| ..Psychomotor Agitation (D011595) 1
| ..Trigonobrachycephaly, Bulbous Bifid Nose, Micrognathia, and Abnormalities of the Hands and Feet (C564759)
|
Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
|
|
|
Term ID: | 4837 |
Name: | Growth Retardation, Small and Puffy Hands and Feet, and Eczema |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D004485|MESH:D005532|MESH:D006130|MESH:D006228|MESH:D011596 |
TreeNumbers: | C05.330.495/C565528 |C05.390.408/C565528 |C05.660.585.512.380/C565528 |C05.660.585.988.425/C565528 |C10.597.606.881/C565528 |C16.131.621.585.380/C565528 |C16.131.621.585.425/C565528 |C17.800.174.620/C565528 |C17.800.815.620/C565528 |C23.550.393/C565528 |C23.888.59 |
Synonyms: | |
Slim Mappings: | Congenital abnormality|Musculoskeletal disease|Nervous system disease|Pathology (process)|Signs and symptoms|Skin disease |
Reference: |
MedGen: C565528
MeSH: C565528
OMIM: 233810;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
|