Pierre-Robin sequence

Symptom Information:

Symptom ID: HPO:0000201
Synonyms:
Pierre Robin sequence [HPO:0000201]
Robin sequence [HPO:0000201]
Pierre Robin sequence [OMIM:Pierre Robin sequence]
Pierre-Robin sequence [OMIM:Pierre-Robin sequence]
Robin sequence [OMIM:Robin sequence]
Pierre Robin sequence (in males) [OMIM:Pierre Robin sequence (in males)]
Pierre-Robin sequence (1 patient) [OMIM:Pierre-Robin sequence (1 patient)]
Quality:
Cross references:
OMIM: "Pierre Robin sequence" [OMIM:Pierre Robin sequence]
OMIM: "Pierre-Robin sequence" [OMIM:Pierre-Robin sequence]
OMIM: "Robin sequence" [OMIM:Robin sequence]
OMIM: "Pierre Robin sequence (in males)" [OMIM:Pierre Robin sequence (in males)]
OMIM: "Pierre-Robin sequence (1 patient)" [OMIM:Pierre-Robin sequence (1 patient)]
Is a (Direct Parents):
HPO         Abnormality of the mouth
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:
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)