Split hand

Symptom Information:

Symptom ID: HPO:0001171
Synonyms:
Claw hand [HPO:0001171]
Claw hand deformities [HPO:0001171]
Claw hands [HPO:0001171]
Claw-hand deformities [HPO:0001171]
Ectrodactyly (hands) [HPO:0001171]
Split-hand [HPO:0001171]
Absent finger [Orphanet:20540]
Congenital cleft hand [HPO:0001171]
Absent finger (disorder) [Orphanet:20540]
Ectrodactyly (disorder) [Orphanet:20140]
Congenital cleft hand (disorder) [Orphanet:20140]
Ectrodactyly [Orphanet:20140]
Claw hand [OMIM:Claw hand]
Claw hand deformities [OMIM:Claw hand deformities]
Claw hands [OMIM:Claw hands]
Claw-hand deformities [OMIM:Claw-hand deformities]
Split hand [OMIM:Split hand]
Split-hand [OMIM:Split-hand]
Oligodactyly/ectrodactyly of fingers [Orphanet:20540]
Trident hand/split hand/abnormal median ray [Orphanet:20140]
Oligodactyly [Orphanet:20540]
Congenital cleft hand [Orphanet:20140]
Adactyly [MedDRA:10049207]
Oligodactyly [MedDRA:10049207]
Congenital cleft hand [MedDRA:10010418]
Cleft hand, congenital [MedDRA:10010418]
Claw hand deformities (in severe cases) [OMIM:Claw hand deformities (in severe cases)]
Claw hand deformity [OMIM:Claw hand deformity]
Claw-hand deformity [OMIM:Claw-hand deformity]
Oligodactyly (45%) [OMIM:Oligodactyly (45%)]
Quality:
Cross references:
HPO:0009380 "Aplasia of the fingers" [Orphanet:20540]
HPO:0001180 "Oligodactyly (hands)" [Orphanet:20540]
Orphanet:20540 "Oligodactyly/ectrodactyly of fingers" [Orphanet:20540]
Orphanet:20140 "Trident hand/split hand/abnormal median ray" [Orphanet:20140]
OMIM: "Claw hand" [OMIM:Claw hand]
OMIM: "Claw hand deformities" [OMIM:Claw hand deformities]
OMIM: "Claw hands" [OMIM:Claw hands]
OMIM: "Claw-hand deformities" [OMIM:Claw-hand deformities]
OMIM: "Split hand" [OMIM:Split hand]
OMIM: "Split-hand" [OMIM:Split-hand]
OMIM: "Claw hand deformities (in severe cases)" [OMIM:Claw hand deformities (in severe cases)]
OMIM: "Claw hand deformity" [OMIM:Claw hand deformity]
OMIM: "Claw-hand deformity" [OMIM:Claw-hand deformity]
OMIM: "Oligodactyly (45%)" [OMIM:Oligodactyly (45%)]
UMLS:C0728895 "Absent finger" [Orphanet:20540]
UMLS:C0265554 "Ectrodactyly" [Orphanet:20140]
Is a (Direct Parents):
MedDRA Musculoskeletal and connective tissue disorders of limbs congenital
HPO         Abnormality of the hand
Orphanet Abnormality of the hand
HPO         Ectrodactyly
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)
                   Ectrodactyly(HPO:0100257)
                      Split hand(HPO:0001171)
                   Abnormality of the upper limb(HPO:0002817)
                      Abnormality of the hand(HPO:0001155)
                         Split hand(HPO:0001171)
MedDRA:
Musculoskeletal and connective tissue disorders(MedDRA:10028395)
    Musculoskeletal and connective tissue disorders congenital(MedDRA:10028396)
       Musculoskeletal and connective tissue disorders of limbs congenital(MedDRA:10028381)
          Split hand(HPO:0001171)
Database Frequency: 72 / 7739
Resource:

All diseases associated with this symptom:

ACRORENAL SYNDROME, AUTOSOMAL RECESSIVE (OMIM:201310)
ADULT syndrome (Orphanet:978)
ANONYCHIA-ECTRODACTYLY (OMIM:106900)
ANONYCHIA-ONYCHODYSTROPHY WITH BRACHYDACTYLY TYPE B AND ECTRODACTYLY (OMIM:106990)
Acro-cardio-facial syndrome (Orphanet:2008)
Acro-renal-mandibular syndrome (Orphanet:958)
Autosomal dominant Charcot-Marie-Tooth disease type 2E (Orphanet:99939)
Autosomal dominant Charcot-Marie-Tooth disease type 2F (Orphanet:99940)
Autosomal dominant Charcot-Marie-Tooth disease type 2K (Orphanet:99944)
Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (Orphanet:93114)
Autosomal recessive Charcot-Marie-Tooth disease with hoarseness (Orphanet:101097)
Autosomal recessive intermediate Charcot-Marie-Tooth disease type A (Orphanet:217055)
BRACHYPHALANGY, POLYDACTYLY, AND TIBIAL APLASIA/HYPOPLASIA (OMIM:609945)
BROWN-VIALETTO-VAN LAERE SYNDROME 2 (OMIM:614707)
Bifunctional enzyme deficiency (Orphanet:300)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMALRECESSIVE (OMIM:607706)
CHARGE syndrome (Orphanet:138)
CHROMOSOME 17p13.3, TELOMERIC, DUPLICATION SYNDROME (OMIM:612576)
Charcot-Marie-Tooth disease type 1A (Orphanet:101081)
Charcot-Marie-Tooth disease type 1B (Orphanet:101082)
Charcot-Marie-Tooth disease type 1E (Orphanet:90658)
Charcot-Marie-Tooth disease type 4A (Orphanet:99948)
Charcot-Marie-Tooth disease type 4B2 (Orphanet:99956)
Congenital cataracts - facial dysmorphism - neuropathy (Orphanet:48431)
Dejerine-Sottas syndrome (Orphanet:64748)
Dermatoosteolysis, Kirghizian type (Orphanet:1657)
Distal hereditary motor neuropathy, Jerash type (Orphanet:139552)
Distal limb deficiencies - micrognathia syndrome (Orphanet:1307)
Dystrophic epidermolysis bullosa (Orphanet:303)
ECTRODACTYLY AND ECTODERMAL DYSPLASIA WITHOUT CLEFT LIP/PALATE (OMIM:129810)
ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE SYNDROME3 (OMIM:604292)
ECTRODACTYLY-CLEFT PALATE SYNDROME (OMIM:129830)
EEC syndrome (Orphanet:1896)
EEM syndrome (Orphanet:1897)
Ectrodactyly - polydactyly (Orphanet:1892)
Focal dermal hypoplasia (Orphanet:2092)
Gollop-Wolfgang complex (Orphanet:1986)
Hurler syndrome (Orphanet:93473)
Hypoglossia - hypodactyly (Orphanet:989)
Intellectual deficit - spasticity - ectrodactyly (Orphanet:1891)
Karsch-Neugebauer syndrome (Orphanet:2329)
Limb-mammary syndrome (Orphanet:69085)
Limited cutaneous systemic sclerosis (Orphanet:220402)
Localized scleroderma (Orphanet:90289)
MUCOLIPIDOSIS III ALPHA/BETA (OMIM:252600)
MUCOLIPIDOSIS III GAMMA (OMIM:252605)
MYOPATHY, DISTAL, 3 (OMIM:610099)
Moebius syndrome (Orphanet:570)
Mucolipidosis type 2 (Orphanet:576)
Mucolipidosis type 3 (Orphanet:577)
Mucopolysaccharidosis type 1 (Orphanet:579)
Mucopolysaccharidosis type 2 (Orphanet:580)
Mucopolysaccharidosis type 6 (Orphanet:583)
Mullerian duct anomalies - limb anomalies (Orphanet:2491)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Patterson-Stevenson-Fontaine syndrome (Orphanet:2439)
Phocomelia - ectrodactyly - deafness - sinus arrhythmia (Orphanet:2878)
Phocomelia, Schinzel type (Orphanet:2879)
SPLIT-HAND AND SPLIT-FOOT WITH HYPODONTIA (OMIM:183500)
SPLIT-HAND/FOOT MALFORMATION 1 (OMIM:183600)
SPLIT-HAND/FOOT MALFORMATION 2 (OMIM:313350)
SPLIT-HAND/FOOT MALFORMATION 4 (OMIM:605289)
SPLIT-HAND/FOOT MALFORMATION 6 (OMIM:225300)
Scheie syndrome (Orphanet:93474)
Split hand - split foot - deafness (Orphanet:71271)
Split hand - urinary anomalies - spina bifida (Orphanet:2437)
Split hand-split foot malformation (Orphanet:2440)
Tetramelic monodactyly (Orphanet:2564)
Tibial aplasia - ectrodactyly (Orphanet:3329)
Torg-Winchester syndrome (Orphanet:3460)
Triphalangeal thumbs - brachyectrodactyly (Orphanet:2947)
Wolf-Hirschhorn syndrome (Orphanet:280)