Pierre-Robin sequence
Symptom Information:
Symptom ID: | HPO:0000201 | |||||||
Synonyms: |
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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) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the face(HPO:0000271) Abnormality of the mouth(HPO:0000153) Pierre-Robin sequence(HPO:0000201) MedDRA: |
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Database Frequency: | 20 / 7739 | |||||||
Resource: |
All diseases associated with this symptom:
Arthrogryposis multiplex congenita - whistling face | (Orphanet:1150) |
Carey-Fineman-Ziter syndrome | (Orphanet:1358) |
Isolated Pierre Robin syndrome | (Orphanet:718) |
Marshall syndrome | (Orphanet:560) |
Osteopathia striata - cranial sclerosis | (Orphanet:2780) |
Otospondylomegaepiphyseal dysplasia | (Orphanet:1427) |
PGM1-CDG | (Orphanet:319646) |
PIERRE ROBIN SEQUENCE WITH PECTUS EXCAVATUM AND RIB AND SCAPULAR ANOMALIES | (OMIM:602196) |
Pierre Robin syndrome - faciodigital anomaly | (Orphanet:2888) |
Richieri Costa-Pereira syndrome | (Orphanet:3102) |
Robin sequence - oligodactyly | (Orphanet:3104) |
STEVENSON-CAREY SYNDROME | (OMIM:611961) |
STICKLER SYNDROME, TYPE I | (OMIM:108300) |
Stickler syndrome | (Orphanet:828) |
Stickler syndrome type 2 | (Orphanet:90654) |
Stickler syndrome type 3 | (Orphanet:166100) |
Toriello-Carey syndrome | (Orphanet:3338) |
VELOCARDIOFACIAL SYNDROME | (OMIM:192430) |
Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence | (Orphanet:3201) |
Weissenbacher- Zweymuller syndrome | (Orphanet:3450) |