Dolichocephaly

Symptom Information:

Symptom ID: HPO:0000268
Synonyms:
Large dolichocephalic skull [HPO:0000268]
Scaphocephaly [HPO:0000268]
Turridolichocephaly [HPO:0000268]
Long narrow head (disorder) [Orphanet:2200]
Scaphycephaly (disorder) [Orphanet:2200]
Long narrow head [Orphanet:2200]
Scaphycephaly [Orphanet:2200]
Dolichocephaly [OMIM:Dolichocephaly]
Large dolichocephalic skull [OMIM:Large dolichocephalic skull]
Scaphocephaly [OMIM:Scaphocephaly]
Turridolichocephaly [OMIM:Turridolichocephaly]
Dolichocephaly/scaphocephaly [Orphanet:2200]
Scaphocephaly [Orphanet:2200]
Scaphocephaly [MedDRA:10049426]
Dolichocephaly (HCS) [OMIM:Dolichocephaly (HCS)]
Dolichocephaly (in 2/4 patients) [OMIM:Dolichocephaly (in 2/4 patients)]
Dolichocephaly (in some patients) [OMIM:Dolichocephaly (in some patients)]
Scaphocephaly (in some patients) [OMIM:Scaphocephaly (in some patients)]
Quality:
Cross references:
Orphanet:2200 "Dolichocephaly/scaphocephaly" [Orphanet:2200]
OMIM: "Dolichocephaly" [OMIM:Dolichocephaly]
OMIM: "Large dolichocephalic skull" [OMIM:Large dolichocephalic skull]
OMIM: "Scaphocephaly" [OMIM:Scaphocephaly]
OMIM: "Turridolichocephaly" [OMIM:Turridolichocephaly]
OMIM: "Dolichocephaly (HCS)" [OMIM:Dolichocephaly (HCS)]
OMIM: "Dolichocephaly (in 2/4 patients)" [OMIM:Dolichocephaly (in 2/4 patients)]
OMIM: "Dolichocephaly (in some patients)" [OMIM:Dolichocephaly (in some patients)]
OMIM: "Scaphocephaly (in some patients)" [OMIM:Scaphocephaly (in some patients)]
UMLS:C0221358 "Dolichocephaly" [HPO:0000268]
UMLS:C0221358 "Long narrow head" [Orphanet:2200]
UMLS:C0265534 "Scaphycephaly" [Orphanet:2200]
Is a (Direct Parents):
MedDRA Musculoskeletal and connective tissue disorders of skull congenital
Orphanet Craniosynostosis
HPO         Abnormality of calvarial morphology
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 skull(HPO:0000929)
                Abnormality of the calvaria(HPO:0002683)
                   Abnormality of calvarial morphology(HPO:0002648)
                      Dolichocephaly(HPO:0000268)
       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 the calvaria(HPO:0002683)
                      Abnormality of calvarial morphology(HPO:0002648)
                         Dolichocephaly(HPO:0000268)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Musculoskeletal and connective tissue disorders of skull congenital(MedDRA:10028382)
          Dolichocephaly(HPO:0000268)
Database Frequency: 144 / 7739
Resource:

All diseases associated with this symptom:

16p13.11 microduplication syndrome (Orphanet:261243)
2p21 microdeletion syndrome (Orphanet:163693)
3M syndrome (Orphanet:2616)
3q13 microdeletion syndrome (Orphanet:1621)
AGENESIS OF THE CORPUS CALLOSUM AND CONGENITAL LYMPHEDEMA (OMIM:613623)
ATP-BINDING CASSETTE, SUBFAMILY D, MEMBER 3 (OMIM:170995)
Acro-renal-mandibular syndrome (Orphanet:958)
Acromesomelic dysplasia, Maroteaux type (Orphanet:40)
Acroosteolysis, dominant type (Orphanet:955)
Aicardi-Goutières syndrome (Orphanet:51)
Alopecia - contractures - dwarfism - intellectual deficit (Orphanet:1005)
Anophthalmia - megalocornea - cardiopathy - skeletal anomalies (Orphanet:1101)
Antenatal multiminicore disease with arthrogryposis multiplex congenita (Orphanet:178148)
Atypical hypotonia - cystinuria syndrome (Orphanet:238523)
Autosomal recessive cutis laxa type 2 (Orphanet:90350)
Autosomal recessive multiple pterygium syndrome (Orphanet:2990)
BASAL GANGLIA CALCIFICATION, IDIOPATHIC, CHILDHOOD-ONSET (OMIM:114100)
Bannayan-Riley-Ruvalcaba syndrome (Orphanet:109)
Beckwith-Wiedemann syndrome due to NSD1 mutation (Orphanet:238613)
Bifunctional enzyme deficiency (Orphanet:300)
Bloom syndrome (Orphanet:125)
Bonnemann-Meinecke-Reich syndrome (Orphanet:1261)
Branchio-oculo-facial syndrome (Orphanet:1297)
CARDIOFACIOCUTANEOUS SYNDROME 1 (OMIM:115150)
CEDNIK syndrome (Orphanet:66631)
CRANIOSYNOSTOSIS WITH OCULAR ABNORMALITIES AND HALLUCAL DEFECTS (OMIM:608279)
CRANIOSYNOSTOSIS-MENTAL RETARDATION SYNDROME OF LIN AND GETTIG (OMIM:218649)
Campomelia, Cumming type (Orphanet:1318)
Cardiocranial syndrome, Pfeiffer type (Orphanet:2872)
Cardiodysrhythmic potassium-sensitive periodic paralysis (Orphanet:37553)
Cardiofaciocutaneous syndrome (Orphanet:1340)
Carpenter-Waziri syndrome (Orphanet:93973)
Childhood-onset hypophosphatasia (Orphanet:247667)
Chudley-Lowry-Hoar syndrome (Orphanet:93971)
Congenital contractural arachnodactyly (Orphanet:115)
Congenital lethal myopathy, Compton-North type (Orphanet:210163)
Cowden syndrome (Orphanet:201)
Cranioectodermal dysplasia (Orphanet:1515)
Cranioectodermal dysplasia 1 (OMIM:218330)
Cranioectodermal dysplasia 2 (OMIM:613610)
Cranioectodermal dysplasia 3 (OMIM:614099)
Craniofacial dyssynostosis (Orphanet:1516)
Craniosynostosis - Dandy-Walker malformation - hydrocephalus (Orphanet:1538)
Craniosynostosis and dental anomalies (Orphanet:284149)
Cryptorchidism - arachnodactyly - intellectual deficit (Orphanet:1548)
Cutis gyrata - acanthosis nigricans - craniosynostosis (Orphanet:1555)
Dandy-Walker malformation - postaxial polydactyly (Orphanet:1566)
Distal monosomy 10q (Orphanet:96148)
Distal trisomy 18q (Orphanet:1716)
Dyssegmental dysplasia - glaucoma (Orphanet:1804)
Familial scaphocephaly syndrome, McGillivray type (Orphanet:168624)
Fanconi anemia (Orphanet:84)
Frontal encephalocele (Orphanet:1931)
German syndrome (Orphanet:2077)
Greig cephalopolysyndactyly syndrome (Orphanet:380)
Hallermann-Streiff syndrome (Orphanet:2108)
Holmes-Gang syndrome (Orphanet:93970)
Hurler syndrome (Orphanet:93473)
Hurler-Scheie syndrome (Orphanet:93476)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
Hypophosphatemic rickets (Orphanet:437)
Hypotonia - cystinuria syndrome (Orphanet:163690)
Isolated oxycephaly (Orphanet:63440)
Isolated scaphocephaly (Orphanet:35093)
Ito hypomelanosis (Orphanet:435)
Joubert syndrome 2 (OMIM:608091)
Juberg-Marsidi syndrome (Orphanet:93972)
LEOPARD SYNDROME 2 (OMIM:611554)
Lateral meningocele syndrome (Orphanet:2789)
Leukocyte adhesion deficiency (Orphanet:2968)
MACROCEPHALY, BENIGN FAMILIAL (OMIM:153470)
MACROCEPHALY/MEGALENCEPHALY SYNDROME, AUTOSOMAL RECESSIVE (OMIM:248000)
MEIER-GORLIN SYNDROME 2 (OMIM:613800)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 15 (OMIM:614202)
MENTAL RETARDATION, AUTOSOMAL RECESSIVE 41 (OMIM:615637)
MENTAL RETARDATION, X-LINKED 72 (OMIM:300271)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 2 (OMIM:614114)
Malignant hyperthermia - arthrogryposis - torticollis (Orphanet:2215)
Marfan syndrome (Orphanet:558)
Marfan syndrome type 1 (Orphanet:284963)
Marfanoid habitus - intellectual deficit, autosomal recessive (Orphanet:2463)
Megalencephaly (Orphanet:2477)
Mesomelic dwarfism, Nievergelt type (Orphanet:2633)
Mevalonic aciduria (Orphanet:29)
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 (Orphanet:2636)
Monosomy 13q14 (Orphanet:1587)
Monosomy 22q13 (Orphanet:48652)
Mosaic trisomy 8 (Orphanet:96061)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mulibrey nanism (Orphanet:2576)
NOONAN SYNDROME 7 (OMIM:613706)
Neonatal adrenoleukodystrophy (Orphanet:44)
Noonan syndrome-like disorder with loose anagen hair (Orphanet:2701)
OCULOCEREBRAL HYPOPIGMENTATION SYNDROME OF PREUS (OMIM:257790)
Oculo-skeletal-renal syndrome (Orphanet:2716)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Oto-onycho-peroneal syndrome (Orphanet:2793)
PEROXISOME BIOGENESIS DISORDER 13A (ZELLWEGER) (OMIM:614887)
PEROXISOME BIOGENESIS DISORDER 2A (ZELLWEGER) (OMIM:214110)
PEROXISOME BIOGENESIS DISORDER 2B (OMIM:202370)
Perlman syndrome (Orphanet:2849)
Polyvalvular heart disease syndrome (Orphanet:228410)
Prader-Willi syndrome (Orphanet:739)
Prominent glabella - microcephaly - hypogenitalism (Orphanet:2083)
Proteus syndrome (Orphanet:744)
Proteus-like syndrome (Orphanet:2969)
RIENHOFF SYNDROME (OMIM:615582)
Radio-ulnar synostosis - intellectual deficit - hypotonia (Orphanet:3270)
Renier-Gabreels-Jasper syndrome (Orphanet:93975)
Richards-Rundle syndrome (Orphanet:1399)
SMITH-MCCORT DYSPLASIA 1 (OMIM:607326)
SOTOS SYNDROME 1 (OMIM:117550)
Sanfilippo syndrome type C (Orphanet:79271)
Schneckenbecken dysplasia (Orphanet:3144)
Short rib-polydactyly syndrome (Orphanet:1505)
Shprintzen-Goldberg syndrome (Orphanet:2462)
Simpson-Golabi-Behmel syndrome type 2 (Orphanet:79022)
Smith-Fineman-Myers syndrome (Orphanet:93974)
Smith-McCort dysplasia (Orphanet:178355)
Sotos syndrome (Orphanet:821)
Spinocerebellar ataxia - dysmorphism (Orphanet:1185)
Spondylocostal dysostosis - anal and genitourinary malformations (Orphanet:94095)
Spondylometaphyseal dysplasia, A4 type (Orphanet:168555)
Suarez-Stickler syndrome (Orphanet:166277)
Syndromic multisystem autoimmune disease due to Itch deficiency (Orphanet:228426)
THAI SYMPHALANGISM SYNDROME (OMIM:608028)
THREE M SYNDROME 1 (OMIM:273750)
THREE M SYNDROME 2 (OMIM:612921)
THREE M SYNDROME 3 (OMIM:614205)
Teebi-Shaltout syndrome (Orphanet:3291)
Temtamy syndrome (Orphanet:1777)
Tetralogy of Fallot (Orphanet:3303)
Thomas syndrome (Orphanet:3316)
Tricho-dento-osseous syndrome (Orphanet:3352)
Triopia (Orphanet:3374)
Trisomy 18 (Orphanet:3380)
Trisomy 20p (Orphanet:261318)
White forelock with malformations (Orphanet:2475)
Wolf-Hirschhorn syndrome (Orphanet:280)
X-linked distal arthrogryposis multiplex congenita (Orphanet:1145)
X-linked intellectual deficit - hypotonic face (Orphanet:73220)
Yunis-Varon syndrome (Orphanet:3472)