Bio2Vec

BIO-KNOWLEDGE-GRAPH

A knowledge graph of biological entities such as genes, gene functions, diseases, phenotypes and chemicals. Embeddings are generated with Walking RDF and OWL method.

Sternocleidomastoid amyotrophy

ID: HP:0012036

Type: http://bio2vec.net/ontology/phenotype

Label: Sternocleidomastoid amyotrophy

Synonyms: Sternocleidomastoid amyotrophy

Alternative IDs: als

API: GO

SPARQL: GO

Similar Entities

Sternocleidomastoid amyotrophy

HP:0012036
Progressive distal muscular atrophy

HP:0008955
Nonprogressive muscular atrophy

HP:0008964
Proximal lower limb amyotrophy

HP:0008956
Generalized amyotrophy

HP:0003700
Pectoralis amyotrophy

HP:0012037
Thigh hypertrophy

HP:0003733
Proximal upper limb muscle hypertrophy

HP:0040266
Lower limb amyotrophy

HP:0007210
Scapuloperoneal amyotrophy

HP:0003697
Proximal amyotrophy

HP:0007126
Generalized limb muscle atrophy

HP:0009055
Upper limb muscle hypertrophy

HP:0040265
Distal lower limb amyotrophy

HP:0008944
Skeletal muscle atrophy

HP:0003202
Aplasia/Hypoplasia of the biceps

HP:0009782
Aplasia of the musculature

HP:0100854
Distal amyotrophy

HP:0003693
Shoulder muscle hypoplasia

HP:0008952
Abnormality of muscle size

HP:0030236
Tibialis atrophy

HP:0011399
Pectoralis hypoplasia

HP:0008998
Biceps aplasia

HP:0009783
Distal upper limb muscle hypertrophy

HP:0040267
obsolete ventral/lateral system

GO:0007353
Aplasia of the pectoralis major muscle

HP:0009751
Interosseus muscle atrophy

HP:0007181
Quadriceps aplasia

HP:0009788
4-nitrophenol 2-monooxygenase activity

GO:0018601
benzothiazole monooxygenase activity

GO:0034859
Pectoral muscle hypoplasia/aplasia

HP:0005258
Aplasia/Hypoplasia involving the musculature of the upper arm

HP:0001468
Aplasia/Hypoplasia of the quadriceps

HP:0009787
Aplasia/Hypoplasia of the musculature of the thigh

HP:0009786
Paraspinal muscle hypertrophy

HP:0012894
Aplasia/Hypoplasia involving the skeletal musculature

HP:0001460
Scapular muscle hypertrophy

HP:0012895
Shoulder girdle muscle atrophy

HP:0003724
Abnormality of the musculature of the thigh

HP:0001441
Quadriceps muscle atrophy

HP:0009050
Aplasia/Hypoplasia involving the shoulder musculature

HP:0001464
Calf muscle hypoplasia

HP:0008962
regulation of pyrimidine-containing compound salvage

GO:1903930
negative regulation of transcription from RNA polymerase II promoter in response to copper ion

GO:0061398
Hypoplasia of deltoid muscle

HP:0030241
Abnormal muscle fiber valosin-containing protein

HP:0030228
Hypoplasia of the musculature

HP:0009004
dibenzofuran 4,4a-dioxygenase activity

GO:0018610
regulation of telomeric RNA transcription from RNA pol II promoter

GO:1901580
PML body organization

GO:0030578
zeaxanthin epoxidase activity

GO:0052662
Aplasia/Hypoplasia involving the musculature of the extremities

HP:0009128
regulation of antigen processing and presentation of peptide or polysaccharide antigen via MHC class II

GO:0002580
dsDNA-RT virus infectious disease

DOID:0050500
regulation of apoptosis involved in tissue homeostasis

GO:0060785
melilotate 3-monooxygenase activity

GO:0050091
regulation of invasive growth in response to glucose limitation

GO:2000217
Hodgkin'\''s sarcoma involving lymph nodes of axilla and upper limb

DOID:9033
Proximal spinal muscular atrophy

HP:0006959
Impaired lymphocyte transformation with phytohemagglutinin

HP:0003347
Progressive spinal muscular atrophy

HP:0009067
argininosuccinate lyase activity

GO:0004056
Hypoplasia of the upper arm musculature

HP:0030239
Generalized muscle hypertrophy

HP:0003720
3-oxoacyl-[acyl-carrier-protein] reductase (NADH) activity

GO:0047025
cytoskeletal matrix organization at active zone

GO:0048789
Lands organization

GO:0030577
F420-0 metabolic process

GO:0052645
Large hyperpigmented retinal spots

HP:0007658
Limb-girdle muscle atrophy

HP:0003797
Abnormal muscle fiber emerin

HP:0030116
regulation of zinc ion transport

GO:0071579
mesenchymal cell apoptotic process involved in nephron morphogenesis

GO:1901145
Segmental spinal muscular atrophy

HP:0009037
Abnormality of the musculature of the upper arm

HP:0001457
Non-midline cleft lip

HP:0100335
Nasal flaring

HP:0030863
Upper limb muscle hypoplasia

HP:0009016
Amyoplasia

HP:0003634
regulation of odontoblast differentiation

GO:1901329
cell cortex of growing cell tip

GO:1902716
Abnormal muscle fiber myotilin

HP:0030226
BMP signaling pathway involved in Malpighian tubule cell chemotaxis

GO:0061353
positive regulation of odontoblast differentiation

GO:1901331
planar cell polarity pathway involved in axis elongation

GO:0003402
Upper limb amyotrophy

HP:0009129
small ribosomal subunit rRNA binding

GO:0070181
Unilateral external ear deformity

HP:0008605
2,4,4-trimethyl-3-oxopentanoate decarboxylase activity

GO:0034853
activin receptor signaling pathway

GO:0032924
regulation of epiboly involved in gastrulation with mouth forming second

GO:1904086
no_name

GO:0052044
recurrent adult primary liver cancer

DOID:7084
no_name

GO:0045441
canonical Wnt signaling pathway involved in neural crest cell differentiation

GO:0044335
Spinal muscular atrophy

HP:0007269
Sperm neck anomaly

HP:0012866
Spinocerebellar tract disease in lower limbs

HP:0007232
BMP signaling pathway involved in renal system segmentation

GO:0061151
regulation of central B cell tolerance induction

GO:0002895

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