01
Diseases
CHROMOSOME 1p32-p31 DELETION SYNDROME
chromosome 1p32-p31 deletion syndrome
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 5
Basic Information
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Core Information
- Disease Name
- CHROMOSOME 1p32-p31 DELETION SYNDROME
- Standard Disease Name
- chromosome 1p32-p31 deletion syndrome
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- C563111
- OMIM ID
- 200130
- UMLS ID
- C0796125
- HPO ID
- No data
Description and Extensions
- Description
- JABL99:A Hallermann-Streiff-like syndrome marked by presenile facies suggesting progeria, absent eyebrows and eyelashes, beaked nose, eye abnormalities, spinal defects, osteoporosis, and other disorders.
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