Narrow palm
Symptom Information:
Symptom ID: | HPO:0004283 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the upper limb(HPO:0002817) Abnormality of the hand(HPO:0001155) Abnormality of the palm(HPO:0100871) Narrow palm(HPO:0004283) MedDRA: |
||||
Database Frequency: | 8 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Cohen syndrome | (Orphanet:193) |
Hypermethioninemia encephalopathy due to adenosine kinase deficiency | (Orphanet:289290) |
Intellectual deficit, X-linked, Snyder type | (Orphanet:3063) |
Koolen-De Vries syndrome | (Orphanet:96169) |
Oculocerebrofacial syndrome, Kaufman type | (Orphanet:2707) |
Prader-Willi syndrome | (Orphanet:739) |
RETINOPATHY, PIGMENTARY, AND MENTAL RETARDATION | (OMIM:268050) |
SCHAAF-YANG SYNDROME | (OMIM:615547) |