Mandibular prognathia
Symptom Information:
Symptom ID: | HPO:0000303 | ||||||||||||||||||||||||||
Synonyms: |
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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 the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal axial skeleton morphology(HPO:0009121) Abnormality of the skull(HPO:0000929) Abnormality of facial skeleton(HPO:0011821) Abnormality of the mandible(HPO:0000277) Mandibular prognathia(HPO:0000303) Abnormality of head or neck(HPO:0000152) Abnormality of the head(HPO:0000234) Abnormality of the skull(HPO:0000929) Abnormality of facial skeleton(HPO:0011821) Abnormality of the mandible(HPO:0000277) Mandibular prognathia(HPO:0000303) Abnormality of the face(HPO:0000271) Abnormality of the chin(HPO:0000306) Mandibular prognathia(HPO:0000303) MedDRA: Musculoskeletal and connective tissue disorders(MedDRA:10028395) Musculoskeletal and connective tissue deformities (incl intervertebral disc disorders)(MedDRA:10028377) Musculoskeletal and connective tissue deformities of skull, face and buccal cavity(MedDRA:10028378) Mandibular prognathia(HPO:0000303) |
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Database Frequency: | 179 / 7739 | ||||||||||||||||||||||||||
Resource: |
All diseases associated with this symptom:
14q12 microdeletion syndrome | (Orphanet:261144) |
17p11.2 microduplication syndrome | (Orphanet:1713) |
17q12 microdeletion syndrome | (Orphanet:261265) |
3M syndrome | (Orphanet:2616) |
ACRODYSOSTOSIS 1 WITH OR WITHOUT HORMONE RESISTANCE | (OMIM:101800) |
ACROMEGALOID CHANGES, CUTIS VERTICIS GYRATA, AND CORNEAL LEUKOMA | (OMIM:102100) |
AREDYLD syndrome | (Orphanet:1133) |
AXENFELD-RIEGER SYNDROME, TYPE 2 | (OMIM:601499) |
Achalasia - microcephaly | (Orphanet:929) |
Acro-fronto-facio-nasal dysostosis | (Orphanet:1784) |
Acrodysostosis | (Orphanet:950) |
Acrodysostosis with multiple hormone resistance | (Orphanet:280651) |
Acromegaly | (Orphanet:963) |
Adenylosuccinate lyase deficiency | (Orphanet:46) |
Alpha-mannosidosis | (Orphanet:61) |
Aminopterin/methotrexate embryofetopathy | (Orphanet:1908) |
Angelman syndrome | (Orphanet:72) |
Anophthalmia - megalocornea - cardiopathy - skeletal anomalies | (Orphanet:1101) |
Aortic arch anomaly - peculiar facies - intellectual deficit | (Orphanet:1110) |
Apert syndrome | (Orphanet:87) |
Aspartylglucosaminuria | (Orphanet:93) |
Autosomal dominant osteosclerosis, Worth type | (Orphanet:2790) |
Autosomal dominant prognathism | (Orphanet:2964) |
Autosomal recessive severe congenital neutropenia due to G6PC3 deficiency | (Orphanet:331176) |
Barber-Say syndrome | (Orphanet:1231) |
Barth syndrome | (Orphanet:111) |
Beckwith-Wiedemann syndrome due to 11p15 microdeletion | (Orphanet:231127) |
Beckwith-Wiedemann syndrome due to 11p15 microduplication | (Orphanet:96076) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
Blepharophimosis - ptosis - esotropia - syndactyly - short stature | (Orphanet:2057) |
Blepharophimosis - radioulnar synostosis | (Orphanet:1256) |
Brachyolmia-amelogenesis imperfecta syndrome | (Orphanet:2899) |
Branchio-skeleto-genital syndrome | (Orphanet:1299) |
CATARACTS, CONGENITAL, WITH SENSORINEURAL DEAFNESS, DOWN SYNDROME-LIKEFACIAL APPEARANCE, SHORT STATURE, AND MENTAL RETARDATION | (OMIM:601088) |
COCKAYNE SYNDROME A | (OMIM:216400) |
COCKAYNE SYNDROME B | (OMIM:133540) |
COCKAYNE SYNDROME, TYPE III | (OMIM:216411) |
CRANIOMETADIAPHYSEAL DYSPLASIA | (OMIM:269300) |
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT | (OMIM:123000) |
CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL RECESSIVE | (OMIM:218400) |
Camptodactyly syndrome, Guadalajara type 1 | (Orphanet:1327) |
Camurati-Engelmann disease | (Orphanet:1328) |
Choanal atresia - deafness - cardiac defects - dysmorphism | (Orphanet:1200) |
Christianson syndrome | (Orphanet:85278) |
Cockayne syndrome | (Orphanet:191) |
Coffin-Lowry syndrome | (Orphanet:192) |
Craniometadiaphyseal dysplasia, wormian bone type | (Orphanet:85184) |
Craniometaphyseal dysplasia | (Orphanet:1522) |
Crouzon disease | (Orphanet:207) |
DYGGVE-MELCHIOR-CLAUSEN DISEASE | (OMIM:223800) |
DYGGVE-MELCHIOR-CLAUSEN SYNDROME, X-LINKED | (OMIM:304950) |
Dental ankylosis | (Orphanet:1077) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Dermo-odonto dysplasia | (Orphanet:1660) |
Developmental delay with autism spectrum disorder and gait instability | (Orphanet:329195) |
Distal 22q11.2 microduplication syndrome | (Orphanet:261337) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
Epidermolysis bullosa simplex with anodontia/hypodontia | (Orphanet:2325) |
Fabry disease | (Orphanet:324) |
Facial dysmorphism - shawl scrotum - joint laxity | (Orphanet:1778) |
Familial osteodysplasia, Anderson type | (Orphanet:2769) |
Familial scaphocephaly syndrome, McGillivray type | (Orphanet:168624) |
Fragile X syndrome | (Orphanet:908) |
Freeman-Sheldon syndrome | (Orphanet:2053) |
GAPO syndrome | (Orphanet:2067) |
GM1 gangliosidosis | (Orphanet:354) |
Geroderma osteodysplastica | (Orphanet:2078) |
Glomerulonephritis - sparse hair - telangiectasis | (Orphanet:2087) |
Gorlin syndrome | (Orphanet:377) |
HYPERPHOSPHATASIA WITH MENTAL RETARDATION SYNDROME 1 | (OMIM:239300) |
Hydrocephalus - costovertebral dysplasia - Sprengel anomaly | (Orphanet:2180) |
Hyperostosis corticalis generalisata | (Orphanet:3416) |
Hyperphosphatasia-intellectual deficiency syndrome | (Orphanet:247262) |
Hypospadias - hypertelorism - coloboma and deafness | (Orphanet:157788) |
Intellectual deficit - athetosis - microphthalmia | (Orphanet:1236) |
Intellectual deficit - dysmorphism - hypogonadism - diabetes mellitus | (Orphanet:3044) |
Intellectual deficit - polydactyly - uncombable hair | (Orphanet:3082) |
Intellectual deficit, Buenos-Aires type | (Orphanet:3079) |
Intellectual deficit, X-linked - Dandy-Walker malformation - basal ganglia disease - Seizures | (Orphanet:1568) |
Intellectual deficit, X-linked - hypogammaglobulinemia - progressive neurological deterioration | (Orphanet:85317) |
Intellectual deficit, X-linked - seizures - psoriasis | (Orphanet:3052) |
Intellectual deficit, X-linked, Armfield type | (Orphanet:85276) |
Intellectual deficit, X-linked, Snyder type | (Orphanet:3063) |
Intellectual deficit, X-linked, Wilson type | (Orphanet:85290) |
Jackson-Weiss syndrome | (Orphanet:1540) |
Kaler-Garrity-Stern syndrome | (Orphanet:2324) |
Kleefstra syndrome | (Orphanet:261494) |
LEOPARD SYNDROME 1 | (OMIM:151100) |
LEOPARD SYNDROME 2 | (OMIM:611554) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 | (OMIM:608594) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 | (OMIM:269700) |
Late-onset localized junctional epidermolysis bullosa - intellectual deficit | (Orphanet:231556) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
Lethal osteosclerotic bone dysplasia | (Orphanet:1832) |
MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE | (OMIM:248000) |
MARFANOID HABITUS WITH SITUS INVERSUS | (OMIM:609008) |
MAXILLOFACIAL DYSOSTOSIS | (OMIM:155000) |
MENTAL RETARDATION, AUTOSOMAL DOMINANT 24 | (OMIM:615828) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41 | (OMIM:615637) |
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 48 | (OMIM:616269) |
MENTAL RETARDATION, OBESITY, MANDIBULAR PROGNATHISM, AND EYE AND SKINANOMALIES | (OMIM:606772) |
MENTAL RETARDATION, X-LINKED 21 | (OMIM:300143) |
MENTAL RETARDATION, X-LINKED, SYNDROMIC 14 | (OMIM:300676) |
MENTAL RETARDATION, X-LINKED, SYNDROMIC, CHUDLEY-SCHWARTZ TYPE | (OMIM:300861) |
MMEP syndrome | (Orphanet:3434) |
MUCOLIPIDOSIS III ALPHA/BETA | (OMIM:252600) |
MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINERECEPTOR DEFICIENCY | (OMIM:608931) |
Macrocephaly - spastic paraplegia - dysmorphism | (Orphanet:2429) |
Maxillo-nasal dysplasia | (Orphanet:1248) |
McCune-Albright syndrome | (Orphanet:562) |
McDonough syndrome | (Orphanet:2471) |
Microbrachycephaly - ptosis - cleft lip | (Orphanet:2511) |
Microcephaly - cleft palate | (Orphanet:2521) |
Microcephaly - glomerulonephritis - marfanoid habitus | (Orphanet:2172) |
Microcephaly - lymphedema - chorioretinopathy | (Orphanet:2526) |
Monosomy 18q | (Orphanet:1600) |
Mowat-Wilson syndrome | (Orphanet:2152) |
Mucolipidosis type 3 | (Orphanet:577) |
Mucopolysaccharidosis type 2 | (Orphanet:580) |
Mucopolysaccharidosis type 2, attenuated form | (Orphanet:217093) |
Mucopolysaccharidosis type 2, severe form | (Orphanet:217085) |
Mucopolysaccharidosis type 4A | (Orphanet:309297) |
Mucopolysaccharidosis type 4B | (Orphanet:309310) |
Myhre syndrome | (Orphanet:2588) |
Nance-Horan syndrome | (Orphanet:627) |
Neurofaciodigitorenal syndrome | (Orphanet:2673) |
Noonan syndrome with multiple lentigines | (Orphanet:500) |
OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2 | (OMIM:259710) |
Oculo-reno-cerebellar syndrome | (Orphanet:2715) |
Oculocerebrorenal syndrome | (Orphanet:534) |
Oculodentodigital dysplasia | (Orphanet:2710) |
Oculoosteocutaneous syndrome | (Orphanet:2713) |
Odonto-tricho-ungual-digito-palmar syndrome | (Orphanet:69082) |
Oro-mandibular-limb hypogenesis syndrome | (Orphanet:2749) |
Osteoglophonic dwarfism | (Orphanet:2645) |
Osteopetrosis | (Orphanet:2781) |
Osteopetrosis with renal tubular acidosis | (Orphanet:2785) |
PERMANENT MOLARS, SECONDARY RETENTION OF | (OMIM:157950) |
Pfeiffer syndrome | (Orphanet:710) |
Pitt-Hopkins-like syndrome 2 | (OMIM:614325) |
Postaxial polydactyly - dental and vertebral anomalies | (Orphanet:2916) |
Progeroid syndrome, Petty type | (Orphanet:2963) |
Proteus-like syndrome | (Orphanet:2969) |
Pyle disease | (Orphanet:3005) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Radial hypoplasia - triphalangeal thumbs - hypospadias - maxillary diastema | (Orphanet:2252) |
Renal cysts and diabetes syndrome | (Orphanet:93111) |
Renpenning syndrome | (Orphanet:3242) |
Rhizomelic dysplasia, Patterson-Lowry type | (Orphanet:2831) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
SCLEROSTEOSIS 1 | (OMIM:269500) |
SCLEROSTEOSIS 2 | (OMIM:614305) |
SOTOS SYNDROME 1 | (OMIM:117550) |
Sakati-Nyhan syndrome | (Orphanet:3128) |
Scalp-ear-nipple syndrome | (Orphanet:2036) |
Scheie syndrome | (Orphanet:93474) |
Sclerosteosis | (Orphanet:3152) |
Severe intellectual deficit - epilepsy - anal anomalies - distal phalangeal hypoplasia | (Orphanet:94066) |
Severe intellectual deficit and progressive spastic paraplegia | (Orphanet:280763) |
Sheldon-Hall syndrome | (Orphanet:1147) |
Short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome | (Orphanet:314394) |
Simpson-Golabi-Behmel syndrome | (Orphanet:373) |
Skeletal dysplasia - epilepsy - short stature | (Orphanet:1858) |
Smith-Magenis syndrome | (Orphanet:819) |
Sotos syndrome | (Orphanet:821) |
Spondyloepimetaphyseal dysplasia, aggrecan type | (Orphanet:171866) |
Syndromic X-linked intellectual deficit due to JARID1C mutation | (Orphanet:85279) |
TENORIO SYNDROME | (OMIM:616260) |
Trismus - pseudocamptodactyly | (Orphanet:3377) |
VAN BUCHEM DISEASE, TYPE 2 | (OMIM:607636) |
W syndrome | (Orphanet:2804) |
Waardenburg syndrome | (Orphanet:3440) |
Waardenburg syndrome type 1 | (Orphanet:894) |
Waardenburg syndrome type 3 | (Orphanet:896) |
Weaver syndrome | (Orphanet:3447) |
Wilson-Turner syndrome | (Orphanet:3459) |
X-linked creatine transporter deficiency | (Orphanet:52503) |
X-linked intellectual deficit - cerebellar hypoplasia | (Orphanet:137831) |
X-linked intellectual deficit with marfanoid habitus | (Orphanet:776) |