Large face
Symptom Information:
Symptom ID: | HPO:0100729 | ||||
Synonyms: |
|
||||
Quality: | |||||
Cross references: |
|
||||
Is a (Direct Parents): |
|
||||
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) Abnormal facial shape(HPO:0001999) Large face(HPO:0100729) MedDRA: |
||||
Database Frequency: | 19 / 7739 | ||||
Resource: |
All diseases associated with this symptom:
Alexander disease | (Orphanet:58) |
Angio-osteohypertrophic syndrome | (Orphanet:2346) |
Aspartylglucosaminuria | (Orphanet:93) |
COLD-INDUCED SWEATING SYNDROME 1 | (OMIM:272430) |
Cartilage-hair hypoplasia | (Orphanet:175) |
Cerebro-oculo-nasal syndrome | (Orphanet:66625) |
Cold-induced sweating syndrome | (Orphanet:157820) |
Corneal anesthesia - deafness - intellectual deficit | (Orphanet:1051) |
Costello syndrome | (Orphanet:3071) |
Distal monosomy 7q36 | (Orphanet:1636) |
Grant syndrome | (Orphanet:2097) |
Hirschsprung disease - nail hypoplasia - dysmorphism | (Orphanet:2153) |
Hurler syndrome | (Orphanet:93473) |
Mesomelic dwarfism, Nievergelt type | (Orphanet:2633) |
PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER) | (OMIM:614883) |
Recombinant 8 syndrome | (Orphanet:96167) |
Rhizomelic dysplasia, Patterson-Lowry type | (Orphanet:2831) |
Short stature - valvular heart disease - characteristic facies | (Orphanet:2868) |
Smith-Magenis syndrome | (Orphanet:819) |