Disease Browser
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Parent Node: Growth Disorders (D006130) | Parent Node: Progeria (D011371) | ..Starting node ..Progeroid Syndrome, Congenital, Petty Type (C567360)
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Sister Nodes: | ..Acrogeria, gottron type (C538187)
| ..Bird headed dwarfism Montreal type (C535448)
| ..Penttinen-Aula syndrome (C536653)
| ..Petty Laxova Wiedemann syndrome (C537886)
| ..Premature Aging Syndrome, Okamoto Type (C566621)
| ..Progeria short stature pigmented nevi (C536422)
| ..Progeria Syndrome, Childhood-Onset (C567661)
| ..Progeroid Facial Appearance with Hand Anomalies (C566563)
| ..Progeroid Syndrome, Congenital, Petty Type (C567360)
| ..Progeroid syndrome, neonatal (C536423)
| ..Ruvalcaba Churesigaew Myhre syndrome (C537190)
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Human Disease MESH is developed by UMLS. Further data from MedGen, OMIM, CTD
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Term ID: | 9305 |
Name: | Progeroid Syndrome, Congenital, Petty Type |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D006130|MESH:D011371 |
TreeNumbers: | C16.320.565.753/C567360 |C18.452.648.753/C567360 |C23.550.393/C567360 |
Synonyms: | |
Slim Mappings: | Genetic disease (inborn)|Metabolic disease|Pathology (process) |
Reference: |
MedGen: C567360
MeSH: C567360
OMIM: 612289;
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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