Slender build
Symptom Information:
Symptom ID: | HPO:0001533 | ||||
Synonyms: |
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Quality: | |||||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Growth abnormality(HPO:0001507) Abnormality of body weight(HPO:0004323) Decreased body weight(HPO:0004325) Slender build(HPO:0001533) Abnormality of body height(HPO:0000002) Tall stature(HPO:0000098) Slender build(HPO:0001533) MedDRA: |
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Database Frequency: | 11 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
CK syndrome | (Orphanet:251383) |
Camurati-Engelmann disease | (Orphanet:1328) |
Congenital muscular dystrophy, Ullrich type | (Orphanet:75840) |
Congenital myopathy with excess of thin filaments | (Orphanet:98904) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
Mitochondrial DNA deletion syndrome with progressive myopathy | (Orphanet:352470) |
NEMALINE MYOPATHY 2 | (OMIM:256030) |
Nemaline myopathy | (Orphanet:607) |
THORACOLARYNGOPELVIC DYSPLASIA | (OMIM:187760) |
Thoracolaryngopelvic dysplasia | (Orphanet:3317) |
X-linked intellectual disability due to GRIA3 anomalies | (Orphanet:364028) |