Abnormality of the metacarpal bones
Symptom Information:
Symptom ID: | HPO:0001163 | ||
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 the skeletal system(HPO:0000924) Abnormality of skeletal morphology(HPO:0011842) Abnormal appendicular skeleton morphology(HPO:0011844) Abnormality of limb bone morphology(HPO:0002813) Abnormality of the upper limb(HPO:0002817) Abnormality of the hand(HPO:0001155) Abnormality of the metacarpal bones(HPO:0001163) MedDRA: |
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Database Frequency: | 149 / 7739 | ||
Resource: |
All diseases associated with this symptom:
14q22q23 microdeletion syndrome | (Orphanet:264200) |
2q31.1 microdeletion syndrome | (Orphanet:251014) |
2q37 microdeletion syndrome | (Orphanet:1001) |
8q21.11 microdeletion syndrome | (Orphanet:284160) |
Absent thumb - short stature - immunodeficiency | (Orphanet:2951) |
Acro-cardio-facial syndrome | (Orphanet:2008) |
Acro-oto-ocular syndrome | (Orphanet:2980) |
Acrocapitofemoral dysplasia | (Orphanet:63446) |
Acrocraniofacial dysostosis | (Orphanet:949) |
Acrodysostosis | (Orphanet:950) |
Acrofacial dysostosis, Palagonia type | (Orphanet:1787) |
Acromegaloid facial appearance syndrome | (Orphanet:965) |
Acromesomelic dysplasia, Grebe type | (Orphanet:2098) |
Acromicric dysplasia | (Orphanet:969) |
Adams-Oliver syndrome | (Orphanet:974) |
Albers-Schönberg osteopetrosis | (Orphanet:53) |
Aphalangy - hemivertebrae - urogenital-intestinal dysgenesis | (Orphanet:1112) |
Aphalangy - syndactyly - microcephaly | (Orphanet:1113) |
Atrioventricular defect - blepharophimosis -radial defects | (Orphanet:1352) |
Auriculoosteodysplasia | (Orphanet:114) |
Autosomal dominant omodysplasia | (Orphanet:93328) |
Baller-Gerold syndrome | (Orphanet:1225) |
Banki syndrome | (Orphanet:1228) |
Bannayan-Riley-Ruvalcaba syndrome | (Orphanet:109) |
Blepharophimosis - radioulnar synostosis | (Orphanet:1256) |
Boomerang dysplasia | (Orphanet:1263) |
Brachydactyly - arterial hypertension | (Orphanet:1276) |
Brachydactyly - nystagmus - cerebellar ataxia | (Orphanet:1246) |
Brachydactyly - preaxial hallux varus | (Orphanet:1278) |
Brachydactyly type A1 | (Orphanet:93388) |
Brachydactyly type A2 | (Orphanet:93396) |
Brachydactyly type B | (Orphanet:93383) |
Brachydactyly type C | (Orphanet:93384) |
Brachydactyly type E | (Orphanet:93387) |
Brachydactyly-syndactyly, Zhao type | (Orphanet:93409) |
Brachytelephalangy - dysmorphism - Kallmann syndrome | (Orphanet:1295) |
CODAS syndrome | (Orphanet:1458) |
Cenani-Lenz syndrome | (Orphanet:3258) |
Charlie M syndrome | (Orphanet:1406) |
Chondrodysplasia - disorder of sex development | (Orphanet:1422) |
Chondrodysplasia, Blomstrand type | (Orphanet:50945) |
Cleft palate - short stature - vertebral anomalies | (Orphanet:2015) |
Coffin-Lowry syndrome | (Orphanet:192) |
Congenital absence/hypoplasia of fingers excluding thumb, unilateral | (Orphanet:973) |
Cornelia de Lange syndrome | (Orphanet:199) |
Crouzon syndrome - acanthosis nigricans | (Orphanet:93262) |
Deafness - genital anomalies - metacarpal and metatarsal synostosis | (Orphanet:3224) |
Dermato-cardio-skeletal syndrome, Borrone type | (Orphanet:1266) |
Diastrophic dwarfism | (Orphanet:628) |
Distal limb deficiencies - micrognathia syndrome | (Orphanet:1307) |
Distal monosomy 13q | (Orphanet:1590) |
Distal monosomy 17q | (Orphanet:1597) |
Dyggve-Melchior-Clausen disease | (Orphanet:239) |
Ectrodactyly - polydactyly | (Orphanet:1892) |
Fountain syndrome | (Orphanet:3219) |
Fuhrmann syndrome | (Orphanet:2854) |
Geleophysic dysplasia | (Orphanet:2623) |
Gorlin syndrome | (Orphanet:377) |
Gorlin-Chaudhry-Moss syndrome | (Orphanet:2095) |
Hand-foot-genital syndrome | (Orphanet:2438) |
Heart-hand syndrome type 2 | (Orphanet:1350) |
Heart-hand syndrome type 3 | (Orphanet:1342) |
Hereditary acrokeratotic poikiloderma, Weary type | (Orphanet:2907) |
Holt-Oram syndrome | (Orphanet:392) |
Holzgreve-Wagner-Rehder syndrome | (Orphanet:2167) |
Humero-radio-ulnar synostosis | (Orphanet:3266) |
Hurler-Scheie syndrome | (Orphanet:93476) |
Hypogonadism - mitral valve prolapse - intellectual deficit | (Orphanet:2233) |
Intellectual deficit - sparse hair - brachydactyly | (Orphanet:3051) |
Isolated brachycephaly | (Orphanet:35099) |
Joubert syndrome with orofaciodigital defect | (Orphanet:2754) |
Juberg-Hayward syndrome | (Orphanet:2319) |
Karsch-Neugebauer syndrome | (Orphanet:2329) |
Kindler syndrome | (Orphanet:2908) |
Larsen-like osseous dysplasia - short stature | (Orphanet:2370) |
Laurin-Sandrow syndrome | (Orphanet:2378) |
Lenz-Majewski hyperostotic dwarfism | (Orphanet:2658) |
Leri pleonosteosis | (Orphanet:2900) |
Léri-Weill dyschondrosteosis | (Orphanet:240) |
Marinesco-Sjögren syndrome | (Orphanet:559) |
McKusick-Kaufman syndrome | (Orphanet:2473) |
Mesoaxial synostotic syndactyly with phalangeal reduction | (Orphanet:157801) |
Mesomelia-synostoses syndrome | (Orphanet:2496) |
Mesomelic dwarfism - cleft palate - camptodactyly | (Orphanet:2631) |
Metaphyseal acroscyphodysplasia | (Orphanet:1240) |
Microbrachycephaly - ptosis - cleft lip | (Orphanet:2511) |
Microcephalic osteodysplastic primordial dwarfism types 1 and 3 | (Orphanet:2636) |
Microgastria - limb reduction defect | (Orphanet:2538) |
Microphthalmia with limb anomalies | (Orphanet:1106) |
Moebius syndrome | (Orphanet:570) |
Mononen-Karnes-Senac syndrome | (Orphanet:2565) |
Multicentric carpo-tarsal osteolysis with or without nephropathy | (Orphanet:2774) |
Nance-Horan syndrome | (Orphanet:627) |
Neurofaciodigitorenal syndrome | (Orphanet:2673) |
Non-rhizomelic chondrodysplasia punctata | (Orphanet:176) |
Oculo-skeletal-renal syndrome | (Orphanet:2716) |
Orofaciodigital syndrome type 2 | (Orphanet:2751) |
Osteocraniostenosis | (Orphanet:2763) |
Osteodysplasty, Melnick-Needles type | (Orphanet:2484) |
Otopalatodigital syndrome | (Orphanet:669) |
Otopalatodigital syndrome type 1 | (Orphanet:90650) |
Otopalatodigital syndrome type 2 | (Orphanet:90652) |
Paraplegia - brachydactyly - cone-shaped epiphysis | (Orphanet:2823) |
Phocomelia - ectrodactyly - deafness - sinus arrhythmia | (Orphanet:2878) |
Platyspondylic dysplasia, Torrance type | (Orphanet:85166) |
Postaxial tetramelic oligodactyly | (Orphanet:2730) |
Proximal symphalangism | (Orphanet:3250) |
Pseudoachondroplasia | (Orphanet:750) |
Radial ray hypoplasia - choanal atresia | (Orphanet:3026) |
Refsum disease | (Orphanet:773) |
Renal-genital-middle ear anomalies | (Orphanet:1092) |
Rhizomelic dysplasia, Patterson-Lowry type | (Orphanet:2831) |
Richieri Costa-Pereira syndrome | (Orphanet:3102) |
Roberts syndrome | (Orphanet:3103) |
Robin sequence - oligodactyly | (Orphanet:3104) |
Rothmund-Thomson syndrome | (Orphanet:2909) |
Ruvalcaba syndrome | (Orphanet:3121) |
SPONASTRIME dysplasia | (Orphanet:93357) |
Schinzel-Giedion syndrome | (Orphanet:798) |
Shoulder and girdle defects - familial intellectual deficit | (Orphanet:2580) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |
Spondyloepimetaphyseal dysplasia with multiple dislocations | (Orphanet:93360) |
Spondyloepimetaphyseal dysplasia, Irapa type | (Orphanet:93351) |
Spondylometaphyseal dysplasia, 'corner fracture' type | (Orphanet:93315) |
Spondylometaphyseal dysplasia, Sedaghatian type | (Orphanet:93317) |
Spondyloperipheral dysplasia - short ulna | (Orphanet:1856) |
Stern-Lubinsky-Durrie syndrome | (Orphanet:3194) |
Stickler syndrome type 3 | (Orphanet:166100) |
Summitt syndrome | (Orphanet:3210) |
Syndactyly type 2 | (Orphanet:93403) |
Syndactyly type 4 | (Orphanet:93405) |
Syndactyly type 5 | (Orphanet:93406) |
Syndactyly type 8 | (Orphanet:2498) |
Syndrome with brachydactyly | (Orphanet:69028) |
Talo-patello-scaphoid osteolysis | (Orphanet:50809) |
Tel Hashomer camptodactyly syndrome | (Orphanet:3292) |
Thumb stiffness - brachydactyly - intellectual deficit | (Orphanet:1078) |
Tricho-odonto-onychodysplasia - dominant syndactyly | (Orphanet:3357) |
Triphalangeal thumb - polysyndactyly syndrome | (Orphanet:2950) |
Trisomy 5p | (Orphanet:1742) |
Turner syndrome | (Orphanet:881) |
Ulna metaphyseal dysplasia syndrome | (Orphanet:1837) |
Ulnar-mammary syndrome | (Orphanet:3138) |
Upper limb defect - eye and ear abnormalities | (Orphanet:2489) |
Van den Ende-Gupta syndrome | (Orphanet:2460) |
Ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence | (Orphanet:3201) |
Verloove Vanhorick-Brubakk syndrome | (Orphanet:3429) |
WT limb-blood syndrome | (Orphanet:3466) |
X-linked dominant chondrodysplasia, Chassaing-Lacombe type | (Orphanet:163966) |