Full cheeks
Symptom Information:
Symptom ID: | HPO:0000293 | |||||||||
Synonyms: |
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Quality: | ||||||||||
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 midface(HPO:0000309) Abnormality of the cheek(HPO:0004426) Full cheeks(HPO:0000293) MedDRA: |
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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) |