Dolichocephaly
Symptom Information:
Symptom ID: | HPO:0000268 | ||||||||||||||||||
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 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) |
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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) |