Full cheeks

Symptom Information:

Symptom ID: HPO:0000293
Synonyms:
Chubby cheeks [HPO:0000293]
Puffy cheeks [HPO:0000293]
Cheek [HPO:0000293]
Chubby cheeks [OMIM:Chubby cheeks]
Full cheeks [OMIM:Full cheeks]
Puffy cheeks [OMIM:Puffy cheeks]
Broad cheeks/cherub-like/cherubin face [Orphanet:3200]
Full cheek [OMIM:Full cheek]
Full cheeks (in some patients) [OMIM:Full cheeks (in some patients)]
Quality:
Cross references:
Orphanet:3200 "Broad cheeks/cherub-like/cherubin face" [Orphanet:3200]
OMIM: "Chubby cheeks" [OMIM:Chubby cheeks]
OMIM: "Full cheeks" [OMIM:Full cheeks]
OMIM: "Puffy cheeks" [OMIM:Puffy cheeks]
OMIM: "Full cheek" [OMIM:Full cheek]
OMIM: "Full cheeks (in some patients)" [OMIM:Full cheeks (in some patients)]
UMLS:C0007966 "Cheek" [HPO:0000293]
Is a (Direct Parents):
Orphanet Abnormal facial shape
HPO         Abnormality of the cheek
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 midface(HPO:0000309)
                   Abnormality of the cheek(HPO:0004426)
                      Full cheeks(HPO:0000293)
MedDRA:
Database Frequency: 85 / 7739
Resource:

All diseases associated with this symptom:

10q22.3q23.3 microduplication syndrome (Orphanet:276422)
20p12.3 microdeletion syndrome (Orphanet:261295)
4q21 microdeletion syndrome (Orphanet:238750)
6q16 deletion syndrome (Orphanet:171829)
8q21.11 microdeletion syndrome (Orphanet:284160)
ARTHROGRYPOSIS, DISTAL, WITH HYPOPITUITARISM, MENTAL RETARDATION,AND FACIAL ANOMALIES (OMIM:208080)
ARTHROGRYPOSIS, PERTHES DISEASE, AND UPWARD GAZE PALSY (OMIM:614262)
AURICULOCONDYLAR SYNDROME 3 (OMIM:615706)
Acromegaly (Orphanet:963)
Acroosteolysis, dominant type (Orphanet:955)
Acute infantile liver failure-multisystemic involvement syndrome (Orphanet:370088)
Albright hereditary osteodystrophy (Orphanet:665)
Arthrogryposis multiplex congenita - whistling face (Orphanet:1150)
Autosomal dominant cutis laxa (Orphanet:90348)
Autosomal recessive cutis laxa type 1 (Orphanet:90349)
Baraitser-Winter syndrome (Orphanet:2995)
Barth syndrome (Orphanet:111)
Beckwith-Wiedemann syndrome due to 11p15 microdeletion (Orphanet:231127)
Blepharophimosis-intellectual deficit syndrome, Ohdo type (Orphanet:2728)
Bohring-Opitz syndrome (Orphanet:97297)
COLD-INDUCED SWEATING SYNDROME 1 (OMIM:272430)
CONGENITAL CONTRACTURES OF THE LIMBS AND FACE, HYPOTONIA, AND DEVELOPMENTALDELAY (OMIM:616266)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Catel-Manzke syndrome (Orphanet:1388)
Cleft palate-lateral synechia syndrome (Orphanet:2016)
Cold-induced sweating syndrome (Orphanet:157820)
Costello syndrome (Orphanet:3071)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Cranioectodermal dysplasia 4 (OMIM:614378)
Diastrophic dwarfism (Orphanet:628)
Distal monosomy 7q36 (Orphanet:1636)
Encephalopathy due to sulfite oxidase deficiency (Orphanet:833)
Fountain syndrome (Orphanet:3219)
Frank-Ter Haar syndrome (Orphanet:137834)
GELEOPHYSIC DYSPLASIA 2 (OMIM:614185)
Geleophysic dysplasia (Orphanet:2623)
Glycogen storage disease due to glucose-6-phosphatase deficiency (Orphanet:364)
Glycogen storage disease due to glycogen debranching enzyme deficiency (Orphanet:366)
HAJDU-CHENEY SYNDROME (OMIM:102500)
Hurler syndrome (Orphanet:93473)
Ichthyosis-cheek-eyebrow syndrome (Orphanet:2267)
Intellectual deficit - hypotonia - skin hyperpigmentation (Orphanet:3050)
LISSENCEPHALY 7 WITH CEREBELLAR HYPOPLASIA (OMIM:616342)
Large congenital melanocytic nevus (Orphanet:626)
MEHMO syndrome (Orphanet:85282)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 27 (OMIM:615866)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type A lipodystrophy (Orphanet:90153)
Meckel syndrome (Orphanet:564)
Megalencephaly-capillary malformation-polymicrogyria syndrome (Orphanet:60040)
Menkes disease (Orphanet:565)
Microcephalic osteodysplastic primordial dwarfism type 2 (Orphanet:2637)
Microcephaly - lymphedema - chorioretinopathy (Orphanet:2526)
Monosomy 22q13 (Orphanet:48652)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 2, attenuated form (Orphanet:217093)
Oculo-palato-cerebral syndrome (Orphanet:2714)
Oculocerebrorenal syndrome (Orphanet:534)
Osteodysplasty, Melnick-Needles type (Orphanet:2484)
Otodental syndrome (Orphanet:2791)
Otofaciocervical syndrome (Orphanet:2792)
PEHO syndrome (Orphanet:2836)
PEHO-like syndrome (Orphanet:99807)
PLANTAR LIPOMATOSIS, UNUSUAL FACIES, AND DEVELOPMENTAL DELAY (OMIM:602342)
Pitt-Hopkins syndrome (Orphanet:2896)
Pontocerebellar hypoplasia type 3 (Orphanet:97249)
Pseudohypoparathyroidism type 1A (Orphanet:79443)
Pseudohypoparathyroidism type 1C (Orphanet:79444)
Pseudopseudohypoparathyroidism (Orphanet:79445)
Ramon syndrome (Orphanet:3019)
STARGARDT MACULAR DEGENERATION, ABSENT OR HYPOPLASTIC CORPUS CALLOSUM,MENTAL RETARDATION, AND DYSMORPHIC FEATURES (OMIM:612948)
Sandhoff disease (Orphanet:796)
Scheie syndrome (Orphanet:93474)
Schwartz-Jampel syndrome (Orphanet:800)
Short-rib thoracic dysplasia 5 with or without polydactyly (OMIM:614376)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type A (Orphanet:308386)
Sulfite oxidase deficiency due to molybdenum cofactor deficiency type B (Orphanet:308393)
Tetrasomy 12p (Orphanet:884)
Toriello-Carey syndrome (Orphanet:3338)
Trisomy 12p (Orphanet:1699)
Trisomy 20p (Orphanet:261318)
Williams syndrome (Orphanet:904)