Long narrow face
Symptom Information:
Symptom ID: | OMIM : No Id available | |||
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Database Frequency: | 11 / 7739 | |||
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All diseases associated with this symptom:
3q29 microdeletion syndrome | (Orphanet:65286) |
BRANCHIOOTORENAL SYNDROME 1 | (OMIM:113650) |
CK syndrome | (Orphanet:251383) |
Christianson syndrome | (Orphanet:85278) |
Marfan syndrome type 1 | (Orphanet:284963) |
Nance-Horan syndrome | (Orphanet:627) |
Oculofaciocardiodental syndrome | (Orphanet:2712) |
Radio-ulnar synostosis - intellectual deficit - hypotonia | (Orphanet:3270) |
Renpenning syndrome | (Orphanet:3242) |
SPASTIC PARAPLEGIA 51, AUTOSOMAL RECESSIVE | (OMIM:613744) |
WEYERS ULNAR RAY/OLIGODACTYLY SYNDROME | (OMIM:602418) |