Normal stature
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 7 / 7739 | ||
Resource: |
All diseases associated with this symptom:
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT | (OMIM:123000) |
CYSTINOSIS, LATE-ONSET JUVENILE OR ADOLESCENT NEPHROPATHIC TYPE | (OMIM:219900) |
Czech dysplasia, metatarsal type | (Orphanet:137678) |
EPIPHYSEAL DYSPLASIA OF FEMORAL HEAD, MYOPIA, AND DEAFNESS | (OMIM:226950) |
EPIPHYSEAL DYSPLASIA, BAUMANN TYPE | (OMIM:610797) |
Multiple epiphyseal dysplasia type 5 | (Orphanet:93311) |
Sanfilippo syndrome type D | (Orphanet:79272) |