Triangular face
Symptom Information:
Symptom ID: | HPO:0000325 | ||||||||
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) Abnormal facial shape(HPO:0001999) Triangular face(HPO:0000325) MedDRA: |
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Database Frequency: | 91 / 7739 | ||||||||
Resource: |
All diseases associated with this symptom:
12q14 microdeletion syndrome | (Orphanet:94063) |
14q11.2 microdeletion syndrome | (Orphanet:261120) |
16q24.3 microdeletion syndrome | (Orphanet:261250) |
17p11.2 microduplication syndrome | (Orphanet:1713) |
17q12 microduplication syndrome | (Orphanet:261272) |
3-hydroxyisobutyric aciduria | (Orphanet:939) |
3M syndrome | (Orphanet:2616) |
Alagille syndrome due to 20p12 microdeletion | (Orphanet:261600) |
Alagille syndrome due to a JAG1 point mutation | (Orphanet:261619) |
Alagille syndrome due to a NOTCH2 point mutation | (Orphanet:261629) |
Aortic arch anomaly - peculiar facies - intellectual deficit | (Orphanet:1110) |
Arthrogryposis with oculomotor limitation and electroretinal anomalies | (Orphanet:1154) |
Autosomal recessive cutis laxa type 2B | (Orphanet:357064) |
Autosomal recessive facio-digito-genital syndrome | (Orphanet:1974) |
BARTTER SYNDROME, ANTENATAL, TYPE 2 | (OMIM:241200) |
Bartter syndrome | (Orphanet:112) |
Brachymorphism - onychodysplasia - dysphalangism | (Orphanet:1292) |
Bruck syndrome | (Orphanet:2771) |
COLE-CARPENTER SYNDROME 2 | (OMIM:616294) |
CREE MENTAL RETARDATION SYNDROME | (OMIM:606851) |
Cardiodysrhythmic potassium-sensitive periodic paralysis | (Orphanet:37553) |
Cataract - deafness - hypogonadism | (Orphanet:1383) |
Caudal appendage - deafness | (Orphanet:1123) |
Cerebellar ataxia - ectodermal dysplasia | (Orphanet:1174) |
Corneal-cerebellar syndrome | (Orphanet:3177) |
Deafness - epiphyseal dysplasia - short stature | (Orphanet:3218) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Distal monosomy 10q | (Orphanet:96148) |
Distal monosomy 15q | (Orphanet:1596) |
Distal monosomy 3p | (Orphanet:1620) |
Distal trisomy 18q | (Orphanet:1716) |
Ehlers-Danlos syndrome, classic type | (Orphanet:287) |
FEINGOLD SYNDROME 1 | (OMIM:164280) |
Feingold syndrome | (Orphanet:1305) |
Fetal Gaucher disease | (Orphanet:85212) |
Floating-Harbor syndrome | (Orphanet:2044) |
GRANDDAD SYNDROME | (OMIM:138920) |
Hennekam-Beemer syndrome | (Orphanet:2135) |
Hypotonia-speech impairment-severe cognitive delay syndrome | (Orphanet:371364) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Intellectual deficit, X-linked - craniofacioskeletal syndrome | (Orphanet:163979) |
Intellectual deficit, X-linked - hypotonia - facial dysmorphism - aggressive behavior | (Orphanet:85329) |
Intellectual deficit, X-linked, Brooks type | (Orphanet:3056) |
KBG syndrome | (Orphanet:2332) |
LEOPARD SYNDROME 1 | (OMIM:151100) |
Legius syndrome | (Orphanet:137605) |
MEIER-GORLIN SYNDROME 3 | (OMIM:613803) |
MEIER-GORLIN SYNDROME 5 | (OMIM:613805) |
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 | (OMIM:614114) |
Mesomelia-synostoses syndrome | (Orphanet:2496) |
Mevalonic aciduria | (Orphanet:29) |
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency | (Orphanet:279934) |
Mosaic variegated aneuploidy syndrome | (Orphanet:1052) |
Mulibrey nanism | (Orphanet:2576) |
Multicentric carpo-tarsal osteolysis with or without nephropathy | (Orphanet:2774) |
Neonatal hemochromatosis | (Orphanet:446) |
Noonan syndrome | (Orphanet:648) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
Noonan syndrome-like disorder with juvenile myelomonocytic leukemia | (Orphanet:363972) |
OSTEOGENESIS IMPERFECTA, TYPE III | (OMIM:259420) |
OSTEOGENESIS IMPERFECTA, TYPE X | (OMIM:613848) |
OSTEOGENESIS IMPERFECTA, TYPE XI | (OMIM:610968) |
OSTEOGENESIS IMPERFECTA, TYPE XIII | (OMIM:614856) |
Osteogenesis imperfecta | (Orphanet:666) |
Osteogenesis imperfecta type 3 | (Orphanet:216812) |
Osteogenesis imperfecta type 5 | (Orphanet:216828) |
PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER) | (OMIM:614883) |
PEROXISOME BIOGENESIS DISORDER 12A (ZELLWEGER) | (OMIM:614886) |
PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER) | (OMIM:614887) |
Partington syndrome | (Orphanet:94083) |
Permanent neonatal diabetes mellitus - pancreatic and cerebellar agenesis | (Orphanet:65288) |
RUIJS-AALFS SYNDROME | (OMIM:616200) |
RUSSELL-SILVER SYNDROME, X-LINKED | (OMIM:312780) |
Renpenning syndrome | (Orphanet:3242) |
Retinal ischemic syndrome - digestive tract small vessel hyalinosis - diffuse cerebral calcifications | (Orphanet:3018) |
SHORT syndrome | (Orphanet:3163) |
Sheldon-Hall syndrome | (Orphanet:1147) |
Short stature, Brussels type | (Orphanet:2867) |
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome | (Orphanet:314394) |
Silver-Russell syndrome | (Orphanet:813) |
THREE M SYNDROME 1 | (OMIM:273750) |
THREE M SYNDROME 2 | (OMIM:612921) |
THREE M SYNDROME 3 | (OMIM:614205) |
Transaldolase deficiency | (Orphanet:101028) |
Trichorhinophalangeal syndrome type 1 and 3 | (Orphanet:77258) |
Trisomy 18 | (Orphanet:3380) |
Wiedemann-Rautenstrauch syndrome | (Orphanet:3455) |
Woodhouse-Sakati syndrome | (Orphanet:3464) |
X-linked intellectual deficit, Golabi-Ito-Hall type | (Orphanet:93947) |
X-linked mandibulofacial dysostosis | (Orphanet:1131) |
Zlotogora-Ogur syndrome | (Orphanet:3253) |