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CER1
No data
- Entity Type
- Diseases
- Relation Groups
- 1
- Relation Preview
- 6
Basic Information
Grouped by core information, identifiers, and descriptions.
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Core Information
- Disease Name
- 9P+ Syndrome
- Standard Disease Name
- 9p+ syndrome
- MeSH Tree
- No data
- ICD-10
- No data
Identifiers
- DO ID
- No data
- MeSH ID
- C538026
- OMIM ID
- No data
- UMLS ID
- C0265428
- HPO ID
- No data
Description and Extensions
- Description
- JABL99:Duplication of the short arm of chromosome 9 with psychomotor retardation, hypertelorism, deep-set eyes, downslanting palpebral fissures, large nose, short upper lip, down-curved corners of the mouth, cup-shaped ears, kyphoscoliosis, small hands and feet, characteristic dermatoglyphic patterns, and cryptorchidism.
Related
Related Entities
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