Triangular face

Symptom Information:

Symptom ID: HPO:0000325
Synonyms:
Triangular facies [HPO:0000325]
Triangular face [OMIM:Triangular face]
Triangular facies [OMIM:Triangular facies]
Triangular face [Orphanet:3120]
Triangular face (in 2/4 patients) [OMIM:Triangular face (in 2/4 patients)]
Triangular face (male) [OMIM:Triangular face (male)]
Triangular face (rare) [OMIM:Triangular face (rare)]
Triangular facies (in some patients) [OMIM:Triangular facies (in some patients)]
Quality:
Cross references:
Orphanet:3120 "Triangular face" [Orphanet:3120]
OMIM: "Triangular face" [OMIM:Triangular face]
OMIM: "Triangular facies" [OMIM:Triangular facies]
OMIM: "Triangular face (in 2/4 patients)" [OMIM:Triangular face (in 2/4 patients)]
OMIM: "Triangular face (male)" [OMIM:Triangular face (male)]
OMIM: "Triangular face (rare)" [OMIM:Triangular face (rare)]
OMIM: "Triangular facies (in some patients)" [OMIM:Triangular facies (in some patients)]
Is a (Direct Parents):
Orphanet Abnormal facial shape
HPO         Abnormal facial shape
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:
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)